KP Pharmaceutical Technology, Inc.
FDA inspection history in Bloomington, Indiana, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Bloomington, Indiana.
Cited most
Across all KP Pharmaceutical Technology observations on file
- 21 CFR 212.20What activities must I perform to ensure drug quality?1
- 21 CFR 212.30What requirements must my facilities and equipment meet?1
The complete KP Pharmaceutical Technology file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Bloomington, Indiana
One Form 483 · 2023 · 2 observations
Latest: Form 483, Feb 3, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-02-03 | 483 Form 483 | Bloomington, Indiana | 2 | $99 |
Investigators on these documents
FEI number 3001802820 · most recent document Feb 3, 2023
About KP Pharmaceutical Technology, Inc.
How many FDA Form 483s has KP Pharmaceutical Technology, Inc. received?
FDA Intel has 1 Form 483 on file for KP Pharmaceutical Technology, Inc.; the most recent is dated Feb 3, 2023.
When was KP Pharmaceutical Technology, Inc. last inspected by FDA?
The most recent FDA inspection document on file for KP Pharmaceutical Technology, Inc. is a Form 483 dated Feb 3, 2023, for the site in Bloomington, Indiana.
What did FDA cite at KP Pharmaceutical Technology, Inc.?
The regulations cited most in the observations on file for KP Pharmaceutical Technology, Inc. are 21 CFR 212.20 (What activities must I perform to ensure drug quality?), 1 time; 21 CFR 212.30 (What requirements must my facilities and equipment meet?), 1 time.