Aquestive Therapeutics
FDA inspection history in Portage, Indiana, 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 Portage, Indiana.
Cited most
Across all Aquestive Therapeutics observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.198Complaint files1
The complete Aquestive Therapeutics file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Portage, Indiana
One Form 483 · 2025 · 2 observations
Latest: Form 483, Jan 30, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-01-30 | 483 Form 483 | Portage, Indiana | 2 | $99 |
Investigators on these documents
FEI number 3004395604 · most recent document Jan 30, 2025
About Aquestive Therapeutics
How many FDA Form 483s has Aquestive Therapeutics received?
FDA Intel has 1 Form 483 on file for Aquestive Therapeutics; the most recent is dated Jan 30, 2025.
When was Aquestive Therapeutics last inspected by FDA?
The most recent FDA inspection document on file for Aquestive Therapeutics is a Form 483 dated Jan 30, 2025, for the site in Portage, Indiana.
What did FDA cite at Aquestive Therapeutics?
The regulations cited most in the observations on file for Aquestive Therapeutics are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.198 (Complaint files), 1 time.