Teva Women's Health LLC
FDA inspection history in Cincinnati, Ohio, 2018 to 2025
- 2
- Form 483s
Every document, by year
- Form 483
2018: one Form 483; 2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Cincinnati, Ohio.
- 2018The longest 483 on file: 4 observations over 4 pages at Cincinnati, Ohio.
- 2025One Form 483, at Cincinnati, Ohio.
Cited most
Across all Teva Women's Health observations on file
- 21 CFR 211.122Materials examination and usage criteria1
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.194Laboratory records1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Teva Women's Health 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
Cincinnati, Ohio
Two Form 483s · 2018 to 2025 · 8 observations
Latest: Form 483, Mar 26, 2025 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-03-26 | 483 Form 483 | Cincinnati, Ohio | 4 | $99 |
| 2018-01-26 | 483 Form 483 | Cincinnati, Ohio | 4 | $99 |
FEI number 1526814 · most recent document Mar 26, 2025
About Teva Women's Health LLC
How many FDA Form 483s has Teva Women's Health LLC received?
FDA Intel has 2 Form 483s on file for Teva Women's Health LLC; the most recent is dated Mar 26, 2025.
When was Teva Women's Health LLC last inspected by FDA?
The most recent FDA inspection document on file for Teva Women's Health LLC is a Form 483 dated Mar 26, 2025, for the site in Cincinnati, Ohio.
What did FDA cite at Teva Women's Health LLC?
The regulations cited most in the observations on file for Teva Women's Health LLC are 21 CFR 211.122 (Materials examination and usage criteria), 1 time; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time.