FDA Investigator Linda A Gregory Duty
Linda A Gregory Duty has conducted inspections on 172 sites in 7 countries as of 16 Oct 2012. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
172
Last Inspection Date:
16 Oct 2012
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America,
Switzerland,
Germany,
United Kingdom of Great Britain and Northern Ireland,
Mexico,
Japan,
Slovenia
FDA Investigators that have inspected at least one site in common with Linda A Gregory Duty:
Abby Lmozeke Baker,
Alissa C Rice,
Althea A Williams,
Amanda M Osteen,
Amber L Adams,
Andrew A Leboeuf,
Andrew Saunders,
Ann B Borromeo,
Anna E Fain,
Arthur S Williams, Jr,
Ashley D Abraham,
Benjamin E Bowen,
Benjamin J Dastoli,
Bonnie E Conley,
Bonnie E Pierson,
Brandon C Heitmeier,
Brian S Lynch,
Byungja E Marciante,
Caitlin L Almonrode,
Carl A Huffman, III,
Carmen M Chan,
Carole Davis,
Carolyn E Barney,
CDR Sean T Creighton,
Charles L Larson,
Charles N Dupont,
Charvais S Hill,
Cherie T Parker,
Cheryl D Mccall,
Cheryl G Scott,
Christine I Shaw,
Christopher J Adams,
Claire M Minden,
Claudette D Brooks,
Clendening,
Clifton C Francis,
Clinton J Lott,
Combs,
Corey K Reno,
Cynthia L Medlin,
Cynthia R Gibson,
Daniel L Aisen,
Danielle M Maddox,
Daphne A Videau,
David J Gallant,
David R Heiar,
Dawn M Braswell,
Dawn P Hall,
Decima L Thompson,
Decima L Washington,
Dianiris C Ayala,
Donna D Gallien, MPH,
Dyanthony T Jenkins,
Edward H Maticka,
Edward R Kay,
Elizabeth D Connell,
Eric R Holm,
Eric W Anderson,
Erica L Sullivan,
Evelyn Taha,
Fabian Nchaparro Rodriguez,
Frank J Marciniak,
Gail L Katz,
George J Flynn,
George T Allen, Jr,
Gisselle I Sensebe,
Gladys B Casper,
Graham N Giesen,
Gregson A Joseph,
Holly M Scott,
Hultman,
Ivy E Sweeney,
Jacqueline S Warner,
Jacquelyn Bradford,
James A Beaulieu,
Jamie P Webb,
Janete F Guardia,
Jason D Abel,
Jesse A Vazquez,
Jessica A Stephens,
Jessica M Simpson, PhD,
Johnathan M Crayton,
Jonathan A Ferguson,
Josiah D Davis,
Juanelma H Palmer,
Juanita Banuelos,
Justin N Henson,
Kari L Batey,
Kari L Norton,
Kathleen S Tormey,
Kelvin Cheung,
Kenneth R Merritt,
Kimberly A Dutzek,
Kimberly L Mcmillan,
Kirtida Patel,
Konsuela Y Glass,
Krista W Whitten,
Kyle J Mccracken,
Lacey J Chessor,
Larry A Estavan,
Laura L Staples,
Laureen M Geniusz,
LCDR Matthew R Mcnew, MPH, REHS/RS,
LCDR Wilfred A Darang,
Leo J Lagrotte,
Leonard H Lavi,
Lindsay H Bertling,
Llopis,
Mahaffey,
Maressa L Mills,
Margaret E Slimbach,
Marissa R Stough,
Mark A Darnell,
Markeesa M Scales,
Marshall H Kinsey,
Mary A Millner,
Matthew B Thomaston,
Maura Rooney,
Mcmillan,
Melanie L Drayton,
Meocha V Whaley,
Mercedes B Mota,
Michael R Duran,
Michelle S Dunaway,
Monica J Wilkins,
Natalie A Guidry,
Natasha N Mccants,
Paige E Shelborne,
Paige E Wilson,
Pamela M Thomas,
Patricia S Smith,
Patrick C Dooley,
Pauline N Logan,
Peggy A Stogner,
Perry H Gambrell,
Randy L Clarida,
Reba A Gates,
Richard L Rutherford,
Ricki A Chase,
Robert E Hultman,
Samuel L Collins,
Sandricka M Mosley,
Sarah M Parkinson,
Shannon Atlas,
Shelton L Stribling,
Shondra N Gipson,
Sidney M Smith,
Stanley B Eugene, BS, BME,
Stephanie A Cochran,
Stephen D Eich,
Stephen G Mclane,
Steven D Dittert,
Susan M Matthias,
Takiyah S Gilmore Embery,
Thanh M Andrews,
Thomas B Smith,
Thomas O Morgan,
Thomas R Stanley,
Traci M Armand,
Tracy J Washington,
Travis E Chapman,
Victor Spanioli,
Wayne S Fortenberry,
Wendy R Blame,
Yehualashet A Gessesse,
Zada L Giles
Linda A Gregory Duty's Documents
Publish Date | Document Type | Title |
---|---|---|
September, 2006 | FDA 483 | Martech Medical Products, Mexico - Form 483, 2006-09-21 |
September, 2002 | FDA 483 Response | Blood Assurance Inc. - Form 483R, 2002-09-18 |
March, 2000 | FDA 483 | Linde Inc. - Form 483, 2000-03-03 |
March, 2000 | EIR | Linde Inc. - EIR, 2000-03-03 |
June, 2004 | FDA 483 | Sterex Electrolysis Int Ltd - Form 483, 2004-06-10 |
January, 2002 | FDA 483 | Pulmonaire Service Inc - Form 483, 2002-01-14 |
September, 2002 | FDA 483 | Blood Assurance Inc. - Form 483, 2002-09-12 |
May, 2001 | EIR | AIRGAS USA, LLC - EIR, 2001-05-31 |
May, 2001 | FDA 483 | AIRGAS USA, LLC - Form 483, 2001-05-31 |
December, 2002 | FDA 483 | Complete Care Inc - Form 483, 2002-12-23 |
April, 2009 | FDA 483 | North American Industrial Manufacturing Company - Form 483, 2009-04-09 |
Experience Redica Systems’ NEW investigator profiles and dashboards
Redica Systems customers get access to over 1,400 FDA Investigator profiles, containing powerful analysis like:
- Total inspections conducted
- 483 rate
- OAI rate
- Warning Letter rate
- Inspections by Industry, Scope, and Inspection Reason
- And much more
Investigator Profiles are not sold as on-demand documents. If you’d like to see one, fill out the form below to connect with our Sales Team and get it in your inbox as little as 24 hours.
Talk to sales to access our investigator profiles
Loading...
Investigator Profiles Are Just the Tip of the Iceberg
Becoming a Redica Systems customer not only provides you with unlimited access to profiles similar to the one above for every current and former FDA Investigator, but also grants you access to:
Inspection Intelligence
- Pre-Approval Inspection (PAI) trends
- The ability to filter nearly any FDA enforcement action by GxP labels like GMP, GCP, etc.
- Latest 483s: see what the trends are across all FDA Investigators
- CFR Heatmap: Citations aggregated by Subpart by Year
Vendor Intelligence
- Full inspection histories for your vendors down to the specific site level
- All of the functionality mentioned above but isolated to just your vendors
Regulatory Intelligence
- Zero in on the trends for a specific agency/regulator (ex. FDA, MHRA, EMA, Health Canada)
- All the latest "Signals" from agencies around the world, segmented by Country, Type (ex. Guidance, Decree...), Category (ex. Rules/Regulations/Guidance, News, Reports...), Theme (ex. Cell and Gene Therapy, AI...), and more