Oxford Pharmaceuticals, LLC
FDA inspection history in Birmingham, Alabama, 2019 to 2023
- 2
- Form 483s
Every document, by year
- Form 483
2019: one Form 483; 2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Birmingham, Alabama.
- 2023One Form 483, at Birmingham, Alabama.
- 2023The longest 483 on file: 4 observations over 4 pages at Birmingham, Alabama.
Cited most
Across all Oxford Pharmaceuticals observations on file
- 21 CFR 211.160General requirements2
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.111Time limitations on production1
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.67(a)Equipment cleaning and maintenance1
The complete Oxford Pharmaceuticals file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Birmingham, Alabama
Two Form 483s · 2019 to 2023 · 7 observations
Latest: Form 483, Nov 3, 2023 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-11-03 | 483 Form 483 | Birmingham, Alabama | 4 | $99 |
| 2019-05-22 | 483 Form 483 | Birmingham, Alabama | 3 | $99 |
Investigators on these documents
FEI number 3012257735 · most recent document Nov 3, 2023
About Oxford Pharmaceuticals, LLC
How many FDA Form 483s has Oxford Pharmaceuticals, LLC received?
FDA Intel has 2 Form 483s on file for Oxford Pharmaceuticals, LLC; the most recent is dated Nov 3, 2023.
When was Oxford Pharmaceuticals, LLC last inspected by FDA?
The most recent FDA inspection document on file for Oxford Pharmaceuticals, LLC is a Form 483 dated Nov 3, 2023, for the site in Birmingham, Alabama.
What did FDA cite at Oxford Pharmaceuticals, LLC?
The regulations cited most in the observations on file for Oxford Pharmaceuticals, LLC are 21 CFR 211.160 (General requirements), 2 times; 21 CFR 211.22 (Responsibilities of quality control unit), 2 times; 21 CFR 211.111 (Time limitations on production), 1 time.