Elementis SRL, Inc.
FDA inspection history in Middletown, New York, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Middletown, New York.
Cited most
Across all Elementis SRL observations on file
- 21 CFR 211.180General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Elementis SRL file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Middletown, New York
One Form 483 · 2022 · 2 observations
Latest: Form 483, Mar 17, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-03-17 | 483 Form 483 | Middletown, New York | 2 | $99 |
Investigators on these documents
FEI number 3006358840 · most recent document Mar 17, 2022
About Elementis SRL, Inc.
How many FDA Form 483s has Elementis SRL, Inc. received?
FDA Intel has 1 Form 483 on file for Elementis SRL, Inc.; the most recent is dated Mar 17, 2022.
When was Elementis SRL, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Elementis SRL, Inc. is a Form 483 dated Mar 17, 2022, for the site in Middletown, New York.
What did FDA cite at Elementis SRL, Inc.?
The regulations cited most in the observations on file for Elementis SRL, Inc. are 21 CFR 211.180 (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.