Steri-Med Pharma Inc.
FDA inspection history in Upton, 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 Upton, Canada.
Cited most
Across all Steri-Med Pharma observations on file
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.42Design and construction features1
The complete Steri-Med Pharma file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Upton, Canada
One Form 483 · 2024 · 1 observation
Latest: Form 483, Feb 27, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-02-27 | 483 Form 483 | Upton, Canada | 1 | $99 |
Investigators on these documents
FEI number 3010165586 · most recent document Feb 27, 2024
About Steri-Med Pharma Inc.
How many FDA Form 483s has Steri-Med Pharma Inc. received?
FDA Intel has 1 Form 483 on file for Steri-Med Pharma Inc.; the most recent is dated Feb 27, 2024.
When was Steri-Med Pharma Inc. last inspected by FDA?
The most recent FDA inspection document on file for Steri-Med Pharma Inc. is a Form 483 dated Feb 27, 2024, for the site in Upton, Canada.
What did FDA cite at Steri-Med Pharma Inc.?
The regulations cited most in the observations on file for Steri-Med Pharma Inc. are 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.42 (Design and construction features), 1 time.