Sanofi Winthrop Industrie
FDA inspection history in Lyon, France, 2020
- 1
- Form 483
Every document, by year
- Form 483
2020: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2020One Form 483, at Lyon, France.
Cited most
Across all Sanofi Winthrop Industrie observations on file
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.194Laboratory records1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Sanofi Winthrop Industrie file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Lyon, France
One Form 483 · 2020 · 5 observations
Latest: Form 483, Feb 18, 2020 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-02-18 | 483 Form 483 | Lyon, France | 5 | $99 |
Investigators on these documents
FEI number 3009194033 · most recent document Feb 18, 2020
About Sanofi Winthrop Industrie
How many FDA Form 483s has Sanofi Winthrop Industrie received?
FDA Intel has 1 Form 483 on file for Sanofi Winthrop Industrie; the most recent is dated Feb 18, 2020.
When was Sanofi Winthrop Industrie last inspected by FDA?
The most recent FDA inspection document on file for Sanofi Winthrop Industrie is a Form 483 dated Feb 18, 2020, for the site in Lyon, France.
What did FDA cite at Sanofi Winthrop Industrie?
The regulations cited most in the observations on file for Sanofi Winthrop Industrie are 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time.