Adare Pharmaceuticals, Inc.
FDA inspection history in Vandalia, Ohio, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at Vandalia, Ohio.
Cited most
Across all Adare Pharmaceuticals observations on file
- 21 CFR 211.192Production record review1
The complete Adare Pharmaceuticals file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Vandalia, Ohio
One Form 483 · 2025 · 1 observation
Latest: Form 483, Feb 25, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-02-25 | 483 Form 483 | Vandalia, Ohio | 1 | $99 |
Investigators on these documents
FEI number 1525864 · most recent document Feb 25, 2025
About Adare Pharmaceuticals, Inc.
How many FDA Form 483s has Adare Pharmaceuticals, Inc. received?
FDA Intel has 1 Form 483 on file for Adare Pharmaceuticals, Inc.; the most recent is dated Feb 25, 2025.
When was Adare Pharmaceuticals, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Adare Pharmaceuticals, Inc. is a Form 483 dated Feb 25, 2025, for the site in Vandalia, Ohio.
What did FDA cite at Adare Pharmaceuticals, Inc.?
The regulations cited most in the observations on file for Adare Pharmaceuticals, Inc. are 21 CFR 211.192 (Production record review), 1 time.