MaxPax, LLC
FDA inspection history in Elkhorn, Wisconsin, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Elkhorn, Wisconsin.
Cited most
Across all MaxPax observations on file
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.160General requirements1
The complete MaxPax file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Elkhorn, Wisconsin
One Form 483 · 2019 · 2 observations
Latest: Form 483, Jul 25, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-07-25 | 483 Form 483 | Elkhorn, Wisconsin | 2 | $99 |
Investigators on these documents
FEI number 3130094 · most recent document Jul 25, 2019
About MaxPax, LLC
How many FDA Form 483s has MaxPax, LLC received?
FDA Intel has 1 Form 483 on file for MaxPax, LLC; the most recent is dated Jul 25, 2019.
When was MaxPax, LLC last inspected by FDA?
The most recent FDA inspection document on file for MaxPax, LLC is a Form 483 dated Jul 25, 2019, for the site in Elkhorn, Wisconsin.
What did FDA cite at MaxPax, LLC?
The regulations cited most in the observations on file for MaxPax, LLC are 21 CFR 211.22 (Responsibilities of quality control unit), 2 times; 21 CFR 211.160 (General requirements), 1 time.