PQ Corporation
FDA inspection history in Utica, Illinois, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Utica, Illinois.
Cited most
Across all PQ observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.56Sanitation1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete PQ file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Utica, Illinois
One Form 483 · 2022 · 6 observations
Latest: Form 483, Feb 22, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-02-22 | 483 Form 483 | Utica, Illinois | 6 | $99 |
FEI number 1421453 · most recent document Feb 22, 2022
About PQ Corporation
How many FDA Form 483s has PQ Corporation received?
FDA Intel has 1 Form 483 on file for PQ Corporation; the most recent is dated Feb 22, 2022.
When was PQ Corporation last inspected by FDA?
The most recent FDA inspection document on file for PQ Corporation is a Form 483 dated Feb 22, 2022, for the site in Utica, Illinois.
What did FDA cite at PQ Corporation?
The regulations cited most in the observations on file for PQ Corporation are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.188 (Batch production and control records), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.