Sanofi Winthrop Industrie
FDA inspection history in Aramon, France, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Aramon, France.
Cited most
Across all Sanofi Winthrop Industrie observations on file
- 21 CFR 211.192Production record review2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.160General requirements1
- 21 CFR 211.165Testing and release for distribution1
The complete Sanofi Winthrop Industrie file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Aramon, France
One Form 483 · 2018 · 3 observations
Latest: Form 483, Jul 17, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-07-17 | 483 Form 483 | Aramon, France | 3 | $99 |
Investigators on these documents
FEI number 3002808341 · most recent document Jul 17, 2018
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 Jul 17, 2018.
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 Jul 17, 2018, for the site in Aramon, 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 211.192 (Production record review), 2 times; 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.160 (General requirements), 1 time.