Brio Pharmaceuticals, Inc.
FDA inspection history in Houston, Texas, 2017 to 2026
- 6
- Form 483s
Every document, by year
- Form 483
2017: one amended 483 and one Form 483; 2018: one Form 483; 2019: one Form 483; 2020: one Form 483; 2026: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017–20Four Form 483s and one amended 483, at Houston, Texas.
- 2019The longest 483 on file: 6 observations over 6 pages at Houston, Texas.
- 2026One Form 483, at Houston, Texas.
Cited most
Across all Brio Pharmaceuticals observations on file
- 21 CFR 211.166Stability testing4
- 21 CFR 211.198Complaint files4
- 21 CFR 211.22Responsibilities of quality control unit4
- 21 CFR 211.192Production record review3
- 21 CFR 211.113Control of microbiological contamination2
The complete Brio Pharmaceuticals file.
All 6 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
15% off buying them one by one
Sites
Houston, Texas
Five Form 483s and one amended 483 · 2017 to 2026 · 25 observations
Latest: Form 483, Feb 27, 2026 →
Documents
6 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-02-27 | 483 Form 483 | Houston, Texas | 2 | $99 |
| 2020-01-24 | 483 Form 483 | Houston, Texas | 1 | $99 |
| 2019-07-11 | 483 Form 483 | Houston, Texas | 6 | $99 |
| 2018-10-03 | 483 Form 483 | Houston, Texas | 4 | $99 |
| 2017-04-26 | Amended 483 Amended 483 | Houston, Texas | 6 | $99 |
| 2017-04-26 | 483 Form 483 | Houston, Texas | 6 | $99 |
Investigators on these documents
Stephen D. Brown (3)Camerson E. Moore (2)Shatina R. Alridge (2)Timothy H. Vo (1)
FEI number 1628196 · most recent document Feb 27, 2026
About Brio Pharmaceuticals, Inc.
How many FDA Form 483s has Brio Pharmaceuticals, Inc. received?
FDA Intel has 6 Form 483s on file for Brio Pharmaceuticals, Inc.; the most recent is dated Feb 27, 2026.
When was Brio Pharmaceuticals, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Brio Pharmaceuticals, Inc. is a Form 483 dated Feb 27, 2026, for the site in Houston, Texas.
What did FDA cite at Brio Pharmaceuticals, Inc.?
The regulations cited most in the observations on file for Brio Pharmaceuticals, Inc. are 21 CFR 211.166 (Stability testing), 4 times; 21 CFR 211.198 (Complaint files), 4 times; 21 CFR 211.22 (Responsibilities of quality control unit), 4 times.