Paket Corporation
FDA inspection history in Chicago, Illinois, 2019 to 2025
- 3
- Form 483s
Every document, by year
- Form 483
2019: two Form 483s; 2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019Two Form 483s, at Chicago, Illinois.
- 2025One Form 483, at Chicago, Illinois.
- 2025The longest 483 on file: 5 observations over 23 pages at Chicago, Illinois.
Cited most
Across all Paket observations on file
- 21 CFR 211.100(b)Written procedures; deviations2
- 21 CFR 211.150(b)Distribution procedures2
- 21 CFR 211.186(a)Master production and control records2
- 21 CFR 211.22(d)Responsibilities of quality control unit2
- 21 CFR 211.67(b)Equipment cleaning and maintenance2
The complete Paket file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Chicago, Illinois
Three Form 483s · 2019 to 2025 · 15 observations
Latest: Form 483, Apr 10, 2025 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-04-10 | 483 Form 483 | Chicago, Illinois | 5 | $99 |
| 2019-08-06 | 483 Form 483 | Chicago, Illinois | 5 | $99 |
| 2019-08-06 | 483 Form 483 | Chicago, Illinois | 5 | $99 |
Investigators on these documents
Brian D. Nicholson (1)Daveta L. Bailey (1)Sonya M. Edmonds (1)
FEI number 1416209 · most recent document Apr 10, 2025
About Paket Corporation
How many FDA Form 483s has Paket Corporation received?
FDA Intel has 3 Form 483s on file for Paket Corporation; the most recent is dated Apr 10, 2025.
When was Paket Corporation last inspected by FDA?
The most recent FDA inspection document on file for Paket Corporation is a Form 483 dated Apr 10, 2025, for the site in Chicago, Illinois.
What did FDA cite at Paket Corporation?
The regulations cited most in the observations on file for Paket Corporation are 21 CFR 211.100(b) (Written procedures; deviations), 2 times; 21 CFR 211.150(b) (Distribution procedures), 2 times; 21 CFR 211.186(a) (Master production and control records), 2 times.