Carnegie Pharmaceuticals, LLC
FDA inspection history in Delran, New Jersey, 2021
- 1
- Form 483
Every document, by year
- Form 483
2021: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2021One Form 483, at Delran, New Jersey.
Cited most
Across all Carnegie Pharmaceuticals observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.165Testing and release for distribution1
- 21 CFR 211.80General requirements1
The complete Carnegie Pharmaceuticals file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Delran, New Jersey
One Form 483 · 2021 · 3 observations
Latest: Form 483, Jun 29, 2021 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-06-29 | 483 Form 483 | Delran, New Jersey | 3 | $99 |
Investigators on these documents
FEI number 3011603634 · most recent document Jun 29, 2021
About Carnegie Pharmaceuticals, LLC
How many FDA Form 483s has Carnegie Pharmaceuticals, LLC received?
FDA Intel has 1 Form 483 on file for Carnegie Pharmaceuticals, LLC; the most recent is dated Jun 29, 2021.
When was Carnegie Pharmaceuticals, LLC last inspected by FDA?
The most recent FDA inspection document on file for Carnegie Pharmaceuticals, LLC is a Form 483 dated Jun 29, 2021, for the site in Delran, New Jersey.
What did FDA cite at Carnegie Pharmaceuticals, LLC?
The regulations cited most in the observations on file for Carnegie Pharmaceuticals, LLC are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.165 (Testing and release for distribution), 1 time; 21 CFR 211.80 (General requirements), 1 time.