Boiron
FDA inspection history in Montevrain, 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 Montevrain, France.
Cited most
Across all Boiron observations on file
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.165Testing and release for distribution1
- 21 CFR 211.192Production record review1
- 21 CFR 211.42Design and construction features1
The complete Boiron file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Montevrain, France
One Form 483 · 2024 · 3 observations
Latest: Form 483, Nov 29, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-11-29 | 483 Form 483 | Montevrain, France | 3 | $99 |
FEI number 3004351878 · most recent document Nov 29, 2024
About Boiron
How many FDA Form 483s has Boiron received?
FDA Intel has 1 Form 483 on file for Boiron; the most recent is dated Nov 29, 2024.
When was Boiron last inspected by FDA?
The most recent FDA inspection document on file for Boiron is a Form 483 dated Nov 29, 2024, for the site in Montevrain, France.
What did FDA cite at Boiron?
The regulations cited most in the observations on file for Boiron are 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.165 (Testing and release for distribution), 1 time; 21 CFR 211.192 (Production record review), 1 time.