FDA Inspection
Roquette FreresRoquette Freres – FDA Inspection, Feb 10, 2017
Record Details
This FDA Inspection record concerns Roquette Freres, with an inspection on February 10, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
View Company Profile
ID · 7404a31a-957a-404a-81c4-2269fd16f22b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1010367
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Roquette Freres
5| Date | Classification | Office | Project area |
|---|---|---|---|
| July 21, 2023 | Not classified | Office of Inspections and Investigations | |
| December 4, 2020 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 10, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 29, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| October 23, 2012 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Roquette Freres
- FDA Inspection 1319296 - 2023-07-21
- FDA Inspection 1144006 - 2020-12-04
- FDA Inspection 1094541 - 2017-11-10
- FDA Inspection 932532 - 2015-05-29
- FDA Inspection 810089 - 2012-10-23
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.