FEI 3006624492
FDA inspection history in Richmond, California, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Richmond, California.
Cited most
Across all site observations on file
- 21 CFR 211.113Control of microbiological contamination3
- 21 CFR 211.188Batch production and control records1
The complete site file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Richmond, California
One Form 483 · 2019 · 4 observations
Latest: Form 483, Sep 18, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-09-18 | 483 Form 483 | Richmond, California | 4 | $99 |
Investigators on these documents
FEI number 3006624492 · most recent document Sep 18, 2019
About FEI 3006624492
How many FDA Form 483s has FEI 3006624492 received?
FDA Intel has 1 Form 483 on file for FEI 3006624492; the most recent is dated Sep 18, 2019.
When was FEI 3006624492 last inspected by FDA?
The most recent FDA inspection document on file for FEI 3006624492 is a Form 483 dated Sep 18, 2019, for the site in Richmond, California.
What did FDA cite at FEI 3006624492?
The regulations cited most in the observations on file for FEI 3006624492 are 21 CFR 211.113 (Control of microbiological contamination), 3 times; 21 CFR 211.188 (Batch production and control records), 1 time.