Keystone Industries
FDA inspection history in Gibbstown, New Jersey, 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 Gibbstown, New Jersey.
Cited most
Across all Keystone Industries observations on file
- 21 CFR 211.165(a)Testing and release for distribution1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete Keystone Industries file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Gibbstown, New Jersey
One Form 483 · 2022 · 2 observations
Latest: Form 483, Dec 21, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-12-21 | 483 Form 483 | Gibbstown, New Jersey | 2 | $99 |
Investigators on these documents
FEI number 3010002722 · most recent document Dec 21, 2022
About Keystone Industries
How many FDA Form 483s has Keystone Industries received?
FDA Intel has 1 Form 483 on file for Keystone Industries; the most recent is dated Dec 21, 2022.
When was Keystone Industries last inspected by FDA?
The most recent FDA inspection document on file for Keystone Industries is a Form 483 dated Dec 21, 2022, for the site in Gibbstown, New Jersey.
What did FDA cite at Keystone Industries?
The regulations cited most in the observations on file for Keystone Industries are 21 CFR 211.165(a) (Testing and release for distribution), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.