Cardinal Health 414 LLC

FDA inspection history in Phoenix, Arizona, 2015

1
Form 483

Every document, by year

  • Form 483

2015: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2015One Form 483, at Phoenix, Arizona.

Cited most

Across all Cardinal Health 414 observations on file

  • 21 CFR 212.20(b)
    What activities must I perform to ensure drug quality?
    2
  • 21 CFR 212.50
    What production and process controls must I have?
    1
  • 21 CFR 212.70(c)
    What controls and acceptance criteria must I have for my finished PET drug products?
    1

The complete Cardinal Health 414 file.

All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.

$99

The documents one by one, while the file is prepared

See the documents

Sites

Documents

1 on file, newest first
DateDocumentPrice
2015-10-16483 Form 483$99

FEI number 3008619510 · most recent document Oct 16, 2015

About Cardinal Health 414 LLC

How many FDA Form 483s has Cardinal Health 414 LLC received?

FDA Intel has 1 Form 483 on file for Cardinal Health 414 LLC; the most recent is dated Oct 16, 2015.

When was Cardinal Health 414 LLC last inspected by FDA?

The most recent FDA inspection document on file for Cardinal Health 414 LLC is a Form 483 dated Oct 16, 2015, for the site in Phoenix, Arizona.

What did FDA cite at Cardinal Health 414 LLC?

The regulations cited most in the observations on file for Cardinal Health 414 LLC are 21 CFR 212.20(b) (What activities must I perform to ensure drug quality?), 2 times; 21 CFR 212.50 (What production and process controls must I have?), 1 time; 21 CFR 212.70(c) (What controls and acceptance criteria must I have for my finished PET drug products?), 1 time.