AbbVie Inc.

FDA inspection history in North Chicago, Illinois, 2017 to 2023

3
Form 483s

Every document, by year

  • Form 483

2017: one Form 483; 2018: one Form 483; 2023: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2017–18Two Form 483s, at North Chicago, Illinois.
  2. 2023One Form 483, at North Chicago, Illinois.
  3. 2023The longest 483 on file: 5 observations over 11 pages at North Chicago, Illinois.

Cited most

Across all AbbVie observations on file

The complete AbbVie file.

All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$297

The price of the documents, added to your cart together

Sites

Documents

3 on file, newest first
DateDocumentPrice
2023-01-31483 Form 483$99
2018-07-02483 Form 483$99
2017-12-15483 Form 483$99

FEI number 3009751352 · most recent document Jan 31, 2023

About AbbVie Inc.

How many FDA Form 483s has AbbVie Inc. received?

FDA Intel has 3 Form 483s on file for AbbVie Inc.; the most recent is dated Jan 31, 2023.

When was AbbVie Inc. last inspected by FDA?

The most recent FDA inspection document on file for AbbVie Inc. is a Form 483 dated Jan 31, 2023, for the site in North Chicago, Illinois.

What did FDA cite at AbbVie Inc.?

The regulations cited most in the observations on file for AbbVie Inc. are 21 CFR 211.192 (Production record review), 2 times; 21 CFR 211.22 (Responsibilities of quality control unit), 2 times; 21 CFR 211.100 (Written procedures; deviations), 1 time.