VHA Office of Advanced Manufacturing
FDA inspection history in Seattle, Washington, 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 Seattle, Washington.
Cited most
Across all VHA Office of Advanced Manufacturing observations on file
- 21 CFR 820.100(b)Corrective and preventive action1
- 21 CFR 820.198(a)Complaint files1
- 21 CFR 820.22Quality audit1
- 21 CFR 820.50(a)(3)Purchasing controls1
The complete VHA Office of Advanced Manufacturing file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Seattle, Washington
One Form 483 · 2025 · 4 observations
Latest: Form 483, Jan 23, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-01-23 | 483 Form 483 | Seattle, Washington | 4 | $99 |
Investigators on these documents
FEI number 3004073926 · most recent document Jan 23, 2025
About VHA Office of Advanced Manufacturing
How many FDA Form 483s has VHA Office of Advanced Manufacturing received?
FDA Intel has 1 Form 483 on file for VHA Office of Advanced Manufacturing; the most recent is dated Jan 23, 2025.
When was VHA Office of Advanced Manufacturing last inspected by FDA?
The most recent FDA inspection document on file for VHA Office of Advanced Manufacturing is a Form 483 dated Jan 23, 2025, for the site in Seattle, Washington.
What did FDA cite at VHA Office of Advanced Manufacturing?
The regulations cited most in the observations on file for VHA Office of Advanced Manufacturing are 21 CFR 820.100(b) (Corrective and preventive action), 1 time; 21 CFR 820.198(a) (Complaint files), 1 time; 21 CFR 820.22 (Quality audit), 1 time.