Accupack Midwest

FDA inspection history in Cincinnati, Ohio, 2024

1
Warning letter
1
Form 483

Every document, by year

  • Warning letter
  • Form 483

2024: one warning letter and one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2024One warning letter and one Form 483, at Cincinnati, Ohio.

Cited most

Across all Accupack Midwest observations on file

The complete Accupack Midwest file.

All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$198

The price of the documents, added to your cart together

Sites

Documents

2 on file, newest first
DateDocumentPrice
2024-08-15Warning letter Warning letter$99
2024-02-27483 Form 483$99

Investigators on these documents

Wen Ning Chan (1)

FEI number 1000122754 · most recent document Aug 15, 2024

About Accupack Midwest

How many FDA Form 483s has Accupack Midwest received?

FDA Intel has 1 Form 483 on file for Accupack Midwest; the most recent is dated Feb 27, 2024.

When was Accupack Midwest last inspected by FDA?

The most recent FDA inspection document on file for Accupack Midwest is a Form 483 dated Feb 27, 2024, for the site in Cincinnati, Ohio.

What did FDA cite at Accupack Midwest?

The regulations cited most in the observations on file for Accupack Midwest are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.67(a) (Equipment cleaning and maintenance), 1 time; 21 CFR 211.68(a) (Automatic, mechanical, and electronic equipment), 1 time.

Has Accupack Midwest received an FDA warning letter?

Yes. FDA Intel has 1 FDA warning letter on file for Accupack Midwest; the most recent is dated Aug 15, 2024.