Rottendorf Pharma GmbH
FDA inspection history in Ennigerloh, Germany, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Ennigerloh, Germany.
Cited most
Across all Rottendorf Pharma observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete Rottendorf Pharma file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Ennigerloh, Germany
One Form 483 · 2019 · 1 observation
Latest: Form 483, Feb 21, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-02-21 | 483 Form 483 | Ennigerloh, Germany | 1 | $99 |
Investigators on these documents
FEI number 3003732290 · most recent document Feb 21, 2019
About Rottendorf Pharma GmbH
How many FDA Form 483s has Rottendorf Pharma GmbH received?
FDA Intel has 1 Form 483 on file for Rottendorf Pharma GmbH; the most recent is dated Feb 21, 2019.
When was Rottendorf Pharma GmbH last inspected by FDA?
The most recent FDA inspection document on file for Rottendorf Pharma GmbH is a Form 483 dated Feb 21, 2019, for the site in Ennigerloh, Germany.
What did FDA cite at Rottendorf Pharma GmbH?
The regulations cited most in the observations on file for Rottendorf Pharma GmbH are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.