Provepharm Life Solutions
FDA inspection history in Marseille, France, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Marseille, France.
Cited most
Across all Provepharm Life Solutions observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Provepharm Life Solutions file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Marseille, France
One Form 483 · 2024
Latest: Form 483, Apr 19, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-04-19 | 483 Form 483 | Marseille, France | — | $99 |
FEI number 3017911817 · most recent document Apr 19, 2024
About Provepharm Life Solutions
How many FDA Form 483s has Provepharm Life Solutions received?
FDA Intel has 1 Form 483 on file for Provepharm Life Solutions; the most recent is dated Apr 19, 2024.
When was Provepharm Life Solutions last inspected by FDA?
The most recent FDA inspection document on file for Provepharm Life Solutions is a Form 483 dated Apr 19, 2024, for the site in Marseille, France.
What did FDA cite at Provepharm Life Solutions?
The regulations cited most in the observations on file for Provepharm Life Solutions are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.