FEI 1650151
FDA inspection history in Oklahoma City, Oklahoma, 2021
- 1
- Form 483
Every document, by year
- Form 483
2021: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2021One Form 483, at Oklahoma City, Oklahoma.
Cited most
Across all site observations on file
- 21 CFR 211.160(a)General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.25(a)Personnel qualifications1
The complete site file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Oklahoma City, Oklahoma
One Form 483 · 2021 · 3 observations
Latest: Form 483, Nov 4, 2021 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-11-04 | 483 Form 483 | Oklahoma City, Oklahoma | 3 | $99 |
Investigators on these documents
FEI number 1650151 · most recent document Nov 4, 2021
About FEI 1650151
How many FDA Form 483s has FEI 1650151 received?
FDA Intel has 1 Form 483 on file for FEI 1650151; the most recent is dated Nov 4, 2021.
When was FEI 1650151 last inspected by FDA?
The most recent FDA inspection document on file for FEI 1650151 is a Form 483 dated Nov 4, 2021, for the site in Oklahoma City, Oklahoma.
What did FDA cite at FEI 1650151?
The regulations cited most in the observations on file for FEI 1650151 are 21 CFR 211.160(a) (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.25(a) (Personnel qualifications), 1 time.