Venator Germany GmbH
FDA inspection history in Duisburg, Germany, 2017
- 1
- Form 483
Every document, by year
- Form 483
2017: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at Duisburg, Germany.
Cited most
Across all Venator Germany observations on file
- 21 CFR 211.160General requirements2
- 21 CFR 211.166Stability testing1
- 21 CFR 211.186Master production and control records1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.192Production record review1
The complete Venator Germany file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Duisburg, Germany
One Form 483 · 2017 · 7 observations
Latest: Form 483, Sep 22, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-09-22 | 483 Form 483 | Duisburg, Germany | 7 | $99 |
Investigators on these documents
FEI number 1000180094 · most recent document Sep 22, 2017
About Venator Germany GmbH
How many FDA Form 483s has Venator Germany GmbH received?
FDA Intel has 1 Form 483 on file for Venator Germany GmbH; the most recent is dated Sep 22, 2017.
When was Venator Germany GmbH last inspected by FDA?
The most recent FDA inspection document on file for Venator Germany GmbH is a Form 483 dated Sep 22, 2017, for the site in Duisburg, Germany.
What did FDA cite at Venator Germany GmbH?
The regulations cited most in the observations on file for Venator Germany GmbH are 21 CFR 211.160 (General requirements), 2 times; 21 CFR 211.166 (Stability testing), 1 time; 21 CFR 211.186 (Master production and control records), 1 time.