E-Z-EM Canada Inc.
FDA inspection history in Anjou, Canada, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Anjou, Canada.
Cited most
Across all E-Z-EM Canada observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete E-Z-EM Canada file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Anjou, Canada
One Form 483 · 2023 · 2 observations
Latest: Form 483, Oct 20, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-10-20 | 483 Form 483 | Anjou, Canada | 2 | $99 |
Investigators on these documents
FEI number 3002808342 · most recent document Oct 20, 2023
About E-Z-EM Canada Inc.
How many FDA Form 483s has E-Z-EM Canada Inc. received?
FDA Intel has 1 Form 483 on file for E-Z-EM Canada Inc.; the most recent is dated Oct 20, 2023.
When was E-Z-EM Canada Inc. last inspected by FDA?
The most recent FDA inspection document on file for E-Z-EM Canada Inc. is a Form 483 dated Oct 20, 2023, for the site in Anjou, Canada.
What did FDA cite at E-Z-EM Canada Inc.?
The regulations cited most in the observations on file for E-Z-EM Canada Inc. are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.