PureTek Corporation
FDA inspection history in San Fernando, California, 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 San Fernando, California.
Cited most
Across all PureTek observations on file
- 21 CFR 211.122(d)Materials examination and usage criteria1
- 21 CFR 211.25(a)Personnel qualifications1
The complete PureTek file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
San Fernando, California
One Form 483 · 2025 · 2 observations
Latest: Form 483, Mar 7, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-03-07 | 483 Form 483 | San Fernando, California | 2 | $99 |
Investigators on these documents
FEI number 1000125324 · most recent document Mar 7, 2025
About PureTek Corporation
How many FDA Form 483s has PureTek Corporation received?
FDA Intel has 1 Form 483 on file for PureTek Corporation; the most recent is dated Mar 7, 2025.
When was PureTek Corporation last inspected by FDA?
The most recent FDA inspection document on file for PureTek Corporation is a Form 483 dated Mar 7, 2025, for the site in San Fernando, California.
What did FDA cite at PureTek Corporation?
The regulations cited most in the observations on file for PureTek Corporation are 21 CFR 211.122(d) (Materials examination and usage criteria), 1 time; 21 CFR 211.25(a) (Personnel qualifications), 1 time.