Akorn, Inc.
FDA inspection history in Decatur, Illinois, 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 Decatur, Illinois.
Cited most
Across all Akorn observations on file
- 21 CFR 211.192Production record review1
The complete Akorn file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Decatur, Illinois
One Form 483 · 2020 · 1 observation
Latest: Form 483, Sep 17, 2020 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-09-17 | 483 Form 483 | Decatur, Illinois | 1 | $99 |
Investigators on these documents
FEI number 1419498 · most recent document Sep 17, 2020
About Akorn, Inc.
How many FDA Form 483s has Akorn, Inc. received?
FDA Intel has 1 Form 483 on file for Akorn, Inc.; the most recent is dated Sep 17, 2020.
When was Akorn, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Akorn, Inc. is a Form 483 dated Sep 17, 2020, for the site in Decatur, Illinois.
What did FDA cite at Akorn, Inc.?
The regulations cited most in the observations on file for Akorn, Inc. are 21 CFR 211.192 (Production record review), 1 time.