Liquipak Corporation
FDA inspection history in Alma, Michigan, 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 Alma, Michigan.
Cited most
Across all Liquipak observations on file
- 21 CFR 211.180(e)(2)General requirements1
- 21 CFR 211.67(b)Equipment cleaning and maintenance1
- 21 CFR 211.68(a)Automatic, mechanical, and electronic equipment1
The complete Liquipak file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Alma, Michigan
One Form 483 · 2025 · 3 observations
Latest: Form 483, Oct 16, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-10-16 | 483 Form 483 | Alma, Michigan | 3 | $99 |
Investigators on these documents
FEI number 1815703 · most recent document Oct 16, 2025
About Liquipak Corporation
How many FDA Form 483s has Liquipak Corporation received?
FDA Intel has 1 Form 483 on file for Liquipak Corporation; the most recent is dated Oct 16, 2025.
When was Liquipak Corporation last inspected by FDA?
The most recent FDA inspection document on file for Liquipak Corporation is a Form 483 dated Oct 16, 2025, for the site in Alma, Michigan.
What did FDA cite at Liquipak Corporation?
The regulations cited most in the observations on file for Liquipak Corporation are 21 CFR 211.180(e)(2) (General requirements), 1 time; 21 CFR 211.67(b) (Equipment cleaning and maintenance), 1 time; 21 CFR 211.68(a) (Automatic, mechanical, and electronic equipment), 1 time.