Arkema, Inc.
FDA inspection history in Piffard, New York, 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 Piffard, New York.
Cited most
Across all Arkema observations on file
- 21 CFR 211.180General requirements1
- 21 CFR 211.198Complaint files1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Arkema file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Piffard, New York
One Form 483 · 2021 · 3 observations
Latest: Form 483, Sep 22, 2021 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-09-22 | 483 Form 483 | Piffard, New York | 3 | $99 |
FEI number 1314624 · most recent document Sep 22, 2021
About Arkema, Inc.
How many FDA Form 483s has Arkema, Inc. received?
FDA Intel has 1 Form 483 on file for Arkema, Inc.; the most recent is dated Sep 22, 2021.
When was Arkema, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Arkema, Inc. is a Form 483 dated Sep 22, 2021, for the site in Piffard, New York.
What did FDA cite at Arkema, Inc.?
The regulations cited most in the observations on file for Arkema, Inc. are 21 CFR 211.180 (General requirements), 1 time; 21 CFR 211.198 (Complaint files), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.