Sanofi Winthrop Industrie
FDA inspection history in Tours, 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 Tours, France.
Cited most
Across all Sanofi Winthrop Industrie observations on file
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete Sanofi Winthrop Industrie file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Tours, France
One Form 483 · 2018 · 1 observation
Latest: Form 483, Jun 15, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-06-15 | 483 Form 483 | Tours, France | 1 | $99 |
Investigators on these documents
FEI number 3003282644 · most recent document Jun 15, 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 Jun 15, 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 Jun 15, 2018, for the site in Tours, 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 211.22(d) (Responsibilities of quality control unit), 1 time.