Delpharm Montreal Inc.
FDA inspection history in Pointe-Claire, 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 Pointe-Claire, Canada.
Cited most
Across all Delpharm Montreal observations on file
- 21 CFR 211.68(a)Automatic, mechanical, and electronic equipment2
- 21 CFR 211.160(a)General requirements1
- 21 CFR 211.208Drug product salvaging1
The complete Delpharm Montreal file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Pointe-Claire, Canada
One Form 483 · 2023 · 4 observations
Latest: Form 483, Sep 1, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-09-01 | 483 Form 483 | Pointe-Claire, Canada | 4 | $99 |
Investigators on these documents
FEI number 3002808099 · most recent document Sep 1, 2023
About Delpharm Montreal Inc.
How many FDA Form 483s has Delpharm Montreal Inc. received?
FDA Intel has 1 Form 483 on file for Delpharm Montreal Inc.; the most recent is dated Sep 1, 2023.
When was Delpharm Montreal Inc. last inspected by FDA?
The most recent FDA inspection document on file for Delpharm Montreal Inc. is a Form 483 dated Sep 1, 2023, for the site in Pointe-Claire, Canada.
What did FDA cite at Delpharm Montreal Inc.?
The regulations cited most in the observations on file for Delpharm Montreal Inc. are 21 CFR 211.68(a) (Automatic, mechanical, and electronic equipment), 2 times; 21 CFR 211.160(a) (General requirements), 1 time; 21 CFR 211.208 (Drug product salvaging), 1 time.