IOI Oleo GmbH
FDA inspection history in Witten, Germany, 2020
- 1
- Form 483
Every document, by year
- Form 483
2020: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2020One Form 483, at Witten, Germany.
Cited most
Across all IOI Oleo observations on file
- 21 CFR 211.198Complaint files1
- 21 CFR 211.25Personnel qualifications1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
- 21 CFR 211.80General requirements1
The complete IOI Oleo file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Witten, Germany
One Form 483 · 2020 · 4 observations
Latest: Form 483, Jan 17, 2020 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-01-17 | 483 Form 483 | Witten, Germany | 4 | $99 |
Investigators on these documents
FEI number 3002807213 · most recent document Jan 17, 2020
About IOI Oleo GmbH
How many FDA Form 483s has IOI Oleo GmbH received?
FDA Intel has 1 Form 483 on file for IOI Oleo GmbH; the most recent is dated Jan 17, 2020.
When was IOI Oleo GmbH last inspected by FDA?
The most recent FDA inspection document on file for IOI Oleo GmbH is a Form 483 dated Jan 17, 2020, for the site in Witten, Germany.
What did FDA cite at IOI Oleo GmbH?
The regulations cited most in the observations on file for IOI Oleo GmbH are 21 CFR 211.198 (Complaint files), 1 time; 21 CFR 211.25 (Personnel qualifications), 1 time; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.