FDA Inspection
Deretil, S.A.Deretil, S.A. – FDA Inspection, Mar 24, 2023
Record Details
This FDA Inspection record concerns Deretil, S.A., with an inspection on March 24, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.
View Company Profile
ID · 08600e27-fed5-4bd5-a87c-4af60fbb922b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1203851
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Deretil, S.A.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| March 13, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 8, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 26, 2013 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 1, 2010 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Deretil, S.A.
- FDA Inspection 1132248 - 2019-03-13
- FDA Inspection 956681 - 2016-01-08
- FDA Inspection 850522 - 2013-09-26
- FDA Inspection 674453 - 2010-07-01
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.