OFD Biopharma, LLC
FDA inspection history in Albany, Oregon, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Albany, Oregon.
Cited most
Across all OFD Biopharma observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.192Production record review1
The complete OFD Biopharma file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Albany, Oregon
One Form 483 · 2022 · 3 observations
Latest: Form 483, Jul 1, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-07-01 | 483 Form 483 | Albany, Oregon | 3 | $99 |
Investigators on these documents
FEI number 3022538 · most recent document Jul 1, 2022
About OFD Biopharma, LLC
How many FDA Form 483s has OFD Biopharma, LLC received?
FDA Intel has 1 Form 483 on file for OFD Biopharma, LLC; the most recent is dated Jul 1, 2022.
When was OFD Biopharma, LLC last inspected by FDA?
The most recent FDA inspection document on file for OFD Biopharma, LLC is a Form 483 dated Jul 1, 2022, for the site in Albany, Oregon.
What did FDA cite at OFD Biopharma, LLC?
The regulations cited most in the observations on file for OFD Biopharma, LLC are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time.