SV Labs Corporation
FDA inspection history in Watsonville, 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 Watsonville, California.
Cited most
Across all SV Labs observations on file
- 21 CFR 211.84(d)(1)Testing and approval or rejection of components, drug product containers, and closures2
- 21 CFR 211.180(e)General requirements1
- 21 CFR 211.188(b)(7)Batch production and control records1
- 21 CFR 211.68(b)Automatic, mechanical, and electronic equipment1
The complete SV Labs file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Watsonville, California
One Form 483 · 2025 · 5 observations
Latest: Form 483, Oct 23, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-10-23 | 483 Form 483 | Watsonville, California | 5 | $99 |
Investigators on these documents
FEI number 2936586 · most recent document Oct 23, 2025
About SV Labs Corporation
How many FDA Form 483s has SV Labs Corporation received?
FDA Intel has 1 Form 483 on file for SV Labs Corporation; the most recent is dated Oct 23, 2025.
When was SV Labs Corporation last inspected by FDA?
The most recent FDA inspection document on file for SV Labs Corporation is a Form 483 dated Oct 23, 2025, for the site in Watsonville, California.
What did FDA cite at SV Labs Corporation?
The regulations cited most in the observations on file for SV Labs Corporation are 21 CFR 211.84(d)(1) (Testing and approval or rejection of components, drug product containers, and closures), 2 times; 21 CFR 211.180(e) (General requirements), 1 time; 21 CFR 211.188(b)(7) (Batch production and control records), 1 time.