Uramix Inc
FDA inspection history in Lansdowne, Pennsylvania, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at Lansdowne, Pennsylvania.
Cited most
Across all Uramix observations on file
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
- 21 CFR 820.20(e)Management responsibility1
The complete Uramix file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Lansdowne, Pennsylvania
One Form 483 · 2025 · 2 observations
Latest: Form 483, May 20, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-05-20 | 483 Form 483 | Lansdowne, Pennsylvania | 2 | $99 |
Investigators on these documents
FEI number 3001642379 · most recent document May 20, 2025
About Uramix Inc
How many FDA Form 483s has Uramix Inc received?
FDA Intel has 1 Form 483 on file for Uramix Inc; the most recent is dated May 20, 2025.
When was Uramix Inc last inspected by FDA?
The most recent FDA inspection document on file for Uramix Inc is a Form 483 dated May 20, 2025, for the site in Lansdowne, Pennsylvania.
What did FDA cite at Uramix Inc?
The regulations cited most in the observations on file for Uramix Inc are 21 CFR 803.17 (What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), 1 time; 21 CFR 820.20(e) (Management responsibility), 1 time.