Element Materials Technology Ann Arbor
FDA inspection history in Ann Arbor, Michigan, 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 Ann Arbor, Michigan.
Cited most
Across all Element Materials Technology Ann Arbor observations on file
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.68(b)Automatic, mechanical, and electronic equipment1
The complete Element Materials Technology Ann Arbor file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Ann Arbor, Michigan
One Form 483 · 2022 · 2 observations
Latest: Form 483, Sep 9, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-09-09 | 483 Form 483 | Ann Arbor, Michigan | 2 | $99 |
Investigators on these documents
FEI number 3008808597 · most recent document Sep 9, 2022
About Element Materials Technology Ann Arbor
How many FDA Form 483s has Element Materials Technology Ann Arbor received?
FDA Intel has 1 Form 483 on file for Element Materials Technology Ann Arbor; the most recent is dated Sep 9, 2022.
When was Element Materials Technology Ann Arbor last inspected by FDA?
The most recent FDA inspection document on file for Element Materials Technology Ann Arbor is a Form 483 dated Sep 9, 2022, for the site in Ann Arbor, Michigan.
What did FDA cite at Element Materials Technology Ann Arbor?
The regulations cited most in the observations on file for Element Materials Technology Ann Arbor are 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time; 21 CFR 211.68(b) (Automatic, mechanical, and electronic equipment), 1 time.