FEI 3007208829
FDA inspection history in San Francisco, California, 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 San Francisco, California.
Cited most
Across all site observations on file
- 21 CFR 8031
- 21 CFR 803.50(a)(2)If I am a manufacturer, what reporting requirements apply to me?1
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.30(g)Design controls1
The complete site file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
San Francisco, California
One Form 483 · 2024 · 3 observations
Latest: Form 483, Jul 31, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-07-31 | 483 Form 483 | San Francisco, California | 3 | $99 |
Investigators on these documents
FEI number 3007208829 · most recent document Jul 31, 2024
About FEI 3007208829
How many FDA Form 483s has FEI 3007208829 received?
FDA Intel has 1 Form 483 on file for FEI 3007208829; the most recent is dated Jul 31, 2024.
When was FEI 3007208829 last inspected by FDA?
The most recent FDA inspection document on file for FEI 3007208829 is a Form 483 dated Jul 31, 2024, for the site in San Francisco, California.
What did FDA cite at FEI 3007208829?
The regulations cited most in the observations on file for FEI 3007208829 are 21 CFR 803, 1 time; 21 CFR 803.50(a)(2) (If I am a manufacturer, what reporting requirements apply to me?), 1 time; 21 CFR 820.100(a) (Corrective and preventive action), 1 time.