Serumwerk Bernburg AG
FDA inspection history in Bernburg, Germany, 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 Bernburg, Germany.
Cited most
Across all Serumwerk Bernburg AG observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
The complete Serumwerk Bernburg AG file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Bernburg, Germany
One Form 483 · 2024 · 2 observations
Latest: Form 483, Jun 14, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-06-14 | 483 Form 483 | Bernburg, Germany | 2 | $99 |
Investigators on these documents
FEI number 3003903447 · most recent document Jun 14, 2024
About Serumwerk Bernburg AG
How many FDA Form 483s has Serumwerk Bernburg AG received?
FDA Intel has 1 Form 483 on file for Serumwerk Bernburg AG; the most recent is dated Jun 14, 2024.
When was Serumwerk Bernburg AG last inspected by FDA?
The most recent FDA inspection document on file for Serumwerk Bernburg AG is a Form 483 dated Jun 14, 2024, for the site in Bernburg, Germany.
What did FDA cite at Serumwerk Bernburg AG?
The regulations cited most in the observations on file for Serumwerk Bernburg AG are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time.