Ohm Laboratories Inc.
FDA inspection history in North Brunswick, New Jersey, 2020
- 1
- Form 483
Every document, by year
- Form 483
2020: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2020One Form 483, at North Brunswick, New Jersey.
Cited most
Across all Ohm Laboratories observations on file
- 21 CFR 211.160(a)General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete Ohm Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
North Brunswick, New Jersey
One Form 483 · 2020 · 3 observations
Latest: Form 483, Feb 5, 2020 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-02-05 | 483 Form 483 | North Brunswick, New Jersey | 3 | $99 |
Investigators on these documents
FEI number 3004132058 · most recent document Feb 5, 2020
About Ohm Laboratories Inc.
How many FDA Form 483s has Ohm Laboratories Inc. received?
FDA Intel has 1 Form 483 on file for Ohm Laboratories Inc.; the most recent is dated Feb 5, 2020.
When was Ohm Laboratories Inc. last inspected by FDA?
The most recent FDA inspection document on file for Ohm Laboratories Inc. is a Form 483 dated Feb 5, 2020, for the site in North Brunswick, New Jersey.
What did FDA cite at Ohm Laboratories Inc.?
The regulations cited most in the observations on file for Ohm Laboratories Inc. are 21 CFR 211.160(a) (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.