Delpharm DIjon
FDA inspection history in Quetigny, 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 Quetigny, France.
Cited most
Across all Delpharm DIjon observations on file
- 21 CFR 211.111Time limitations on production1
- 21 CFR 211.186Master production and control records1
The complete Delpharm DIjon file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Quetigny, France
One Form 483 · 2024 · 2 observations
Latest: Form 483, May 31, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-05-31 | 483 Form 483 | Quetigny, France | 2 | $99 |
Investigators on these documents
FEI number 3014120699 · most recent document May 31, 2024
About Delpharm DIjon
How many FDA Form 483s has Delpharm DIjon received?
FDA Intel has 1 Form 483 on file for Delpharm DIjon; the most recent is dated May 31, 2024.
When was Delpharm DIjon last inspected by FDA?
The most recent FDA inspection document on file for Delpharm DIjon is a Form 483 dated May 31, 2024, for the site in Quetigny, France.
What did FDA cite at Delpharm DIjon?
The regulations cited most in the observations on file for Delpharm DIjon are 21 CFR 211.111 (Time limitations on production), 1 time; 21 CFR 211.186 (Master production and control records), 1 time.