Port Jervis Laboratories, Inc
FDA inspection history in Port Jervis, 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 Port Jervis, New York.
Cited most
Across all Port Jervis Laboratories observations on file
- 21 CFR 211.160(b)(4)General requirements1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete Port Jervis Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Port Jervis, New York
One Form 483 · 2022 · 2 observations
Latest: Form 483, Nov 4, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-11-04 | 483 Form 483 | Port Jervis, New York | 2 | $99 |
Investigators on these documents
FEI number 1317131 · most recent document Nov 4, 2022
About Port Jervis Laboratories, Inc
How many FDA Form 483s has Port Jervis Laboratories, Inc received?
FDA Intel has 1 Form 483 on file for Port Jervis Laboratories, Inc; the most recent is dated Nov 4, 2022.
When was Port Jervis Laboratories, Inc last inspected by FDA?
The most recent FDA inspection document on file for Port Jervis Laboratories, Inc is a Form 483 dated Nov 4, 2022, for the site in Port Jervis, New York.
What did FDA cite at Port Jervis Laboratories, Inc?
The regulations cited most in the observations on file for Port Jervis Laboratories, Inc are 21 CFR 211.160(b)(4) (General requirements), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.