EO Products, LLC
FDA inspection history in San Rafael, California, 2020
- 1
- Form 483
Every document, by year
- Form 483
2020: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2020One Form 483, at San Rafael, California.
Cited most
Across all EO Products observations on file
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.84(d)(2)Testing and approval or rejection of components, drug product containers, and closures1
The complete EO Products file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
San Rafael, California
One Form 483 · 2020 · 3 observations
Latest: Form 483, Nov 17, 2020 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-11-17 | 483 Form 483 | San Rafael, California | 3 | $99 |
Investigators on these documents
FEI number 2915875 · most recent document Nov 17, 2020
About EO Products, LLC
How many FDA Form 483s has EO Products, LLC received?
FDA Intel has 1 Form 483 on file for EO Products, LLC; the most recent is dated Nov 17, 2020.
When was EO Products, LLC last inspected by FDA?
The most recent FDA inspection document on file for EO Products, LLC is a Form 483 dated Nov 17, 2020, for the site in San Rafael, California.
What did FDA cite at EO Products, LLC?
The regulations cited most in the observations on file for EO Products, LLC are 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time; 21 CFR 211.84(d)(2) (Testing and approval or rejection of components, drug product containers, and closures), 1 time.