Regis Technologies Inc.
FDA inspection history in Morton Grove, 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 Morton Grove, Illinois.
Cited most
Across all Regis Technologies observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.89Rejected components, drug product containers, and closures1
The complete Regis Technologies file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Morton Grove, Illinois
One Form 483 · 2022 · 2 observations
Latest: Form 483, Nov 16, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-11-16 | 483 Form 483 | Morton Grove, Illinois | 2 | $99 |
FEI number 1416120 · most recent document Nov 16, 2022
About Regis Technologies Inc.
How many FDA Form 483s has Regis Technologies Inc. received?
FDA Intel has 1 Form 483 on file for Regis Technologies Inc.; the most recent is dated Nov 16, 2022.
When was Regis Technologies Inc. last inspected by FDA?
The most recent FDA inspection document on file for Regis Technologies Inc. is a Form 483 dated Nov 16, 2022, for the site in Morton Grove, Illinois.
What did FDA cite at Regis Technologies Inc.?
The regulations cited most in the observations on file for Regis Technologies Inc. are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time; 21 CFR 211.89 (Rejected components, drug product containers, and closures), 1 time.