Juno Pharma Canada Inc.
FDA inspection history in Montreal, Canada, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Montreal, Canada.
Cited most
Across all Juno Pharma Canada observations on file
- 21 CFR 211.63Equipment design, size, and location1
- 21 CFR 211.67(a)Equipment cleaning and maintenance1
The complete Juno Pharma Canada file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Montreal, Canada
One Form 483 · 2024 · 2 observations
Latest: Form 483, Jan 17, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-01-17 | 483 Form 483 | Montreal, Canada | 2 | $99 |
Investigators on these documents
FEI number 3004153143 · most recent document Jan 17, 2024
About Juno Pharma Canada Inc.
How many FDA Form 483s has Juno Pharma Canada Inc. received?
FDA Intel has 1 Form 483 on file for Juno Pharma Canada Inc.; the most recent is dated Jan 17, 2024.
When was Juno Pharma Canada Inc. last inspected by FDA?
The most recent FDA inspection document on file for Juno Pharma Canada Inc. is a Form 483 dated Jan 17, 2024, for the site in Montreal, Canada.
What did FDA cite at Juno Pharma Canada Inc.?
The regulations cited most in the observations on file for Juno Pharma Canada Inc. are 21 CFR 211.63 (Equipment design, size, and location), 1 time; 21 CFR 211.67(a) (Equipment cleaning and maintenance), 1 time.