Omya Inc.
FDA inspection history in Superior, Arizona, 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 Superior, Arizona.
Cited most
Across all Omya observations on file
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete Omya file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Superior, Arizona
One Form 483 · 2022 · 2 observations
Latest: Form 483, May 27, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-05-27 | 483 Form 483 | Superior, Arizona | 2 | $99 |
Investigators on these documents
FEI number 3003624292 · most recent document May 27, 2022
About Omya Inc.
How many FDA Form 483s has Omya Inc. received?
FDA Intel has 1 Form 483 on file for Omya Inc.; the most recent is dated May 27, 2022.
When was Omya Inc. last inspected by FDA?
The most recent FDA inspection document on file for Omya Inc. is a Form 483 dated May 27, 2022, for the site in Superior, Arizona.
What did FDA cite at Omya Inc.?
The regulations cited most in the observations on file for Omya Inc. are 21 CFR 211.22 (Responsibilities of quality control unit), 1 time; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.