Apozeal Pharmaceuticals Inc
FDA inspection history in Levittown, Pennsylvania, 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 Levittown, Pennsylvania.
Cited most
Across all Apozeal Pharmaceuticals observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.67Equipment cleaning and maintenance1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete Apozeal Pharmaceuticals file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Levittown, Pennsylvania
One Form 483 · 2025 · 5 observations
Latest: Form 483, Oct 15, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-10-15 | 483 Form 483 | Levittown, Pennsylvania | 5 | $99 |
Investigators on these documents
FEI number 3004536946 · most recent document Oct 15, 2025
About Apozeal Pharmaceuticals Inc
How many FDA Form 483s has Apozeal Pharmaceuticals Inc received?
FDA Intel has 1 Form 483 on file for Apozeal Pharmaceuticals Inc; the most recent is dated Oct 15, 2025.
When was Apozeal Pharmaceuticals Inc last inspected by FDA?
The most recent FDA inspection document on file for Apozeal Pharmaceuticals Inc is a Form 483 dated Oct 15, 2025, for the site in Levittown, Pennsylvania.
What did FDA cite at Apozeal Pharmaceuticals Inc?
The regulations cited most in the observations on file for Apozeal Pharmaceuticals Inc are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.