Apex Pharmaceuticals, Inc.
FDA inspection history in South Plainfield, New Jersey, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at South Plainfield, New Jersey.
Cited most
Across all Apex Pharmaceuticals observations on file
- 21 CFR 211.67Equipment cleaning and maintenance5
- 21 CFR 211.160(b)General requirements1
The complete Apex Pharmaceuticals file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
South Plainfield, New Jersey
One Form 483 · 2019 · 3 observations
Latest: Form 483, Apr 18, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-04-18 | 483 Form 483 | South Plainfield, New Jersey | 3 | $99 |
Investigators on these documents
FEI number 3006719767 · most recent document Apr 18, 2019
About Apex Pharmaceuticals, Inc.
How many FDA Form 483s has Apex Pharmaceuticals, Inc. received?
FDA Intel has 1 Form 483 on file for Apex Pharmaceuticals, Inc.; the most recent is dated Apr 18, 2019.
When was Apex Pharmaceuticals, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Apex Pharmaceuticals, Inc. is a Form 483 dated Apr 18, 2019, for the site in South Plainfield, New Jersey.
What did FDA cite at Apex Pharmaceuticals, Inc.?
The regulations cited most in the observations on file for Apex Pharmaceuticals, Inc. are 21 CFR 211.67 (Equipment cleaning and maintenance), 5 times; 21 CFR 211.160(b) (General requirements), 1 time.