Kerber USA Inc
FDA inspection history in Amherst, New York, 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 Amherst, New York.
Cited most
Across all Kerber USA observations on file
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.184Device history record1
- 21 CFR 820.198(a)Complaint files1
- 21 CFR 820.22Quality audit1
- 21 CFR 820.30(a)Design controls1
The complete Kerber USA file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Amherst, New York
One Form 483 · 2022 · 7 observations
Latest: Form 483, Nov 2, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-11-02 | 483 Form 483 | Amherst, New York | 7 | $99 |
Investigators on these documents
FEI number 3017419219 · most recent document Nov 2, 2022
About Kerber USA Inc
How many FDA Form 483s has Kerber USA Inc received?
FDA Intel has 1 Form 483 on file for Kerber USA Inc; the most recent is dated Nov 2, 2022.
When was Kerber USA Inc last inspected by FDA?
The most recent FDA inspection document on file for Kerber USA Inc is a Form 483 dated Nov 2, 2022, for the site in Amherst, New York.
What did FDA cite at Kerber USA Inc?
The regulations cited most in the observations on file for Kerber USA Inc are 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.184 (Device history record), 1 time; 21 CFR 820.198(a) (Complaint files), 1 time.