Evonik Corporation

FDA inspection history in Birmingham, Alabama, 2018 to 2024

3
Form 483s

Every document, by year

  • Form 483

2018: one Form 483; 2020: one Form 483; 2024: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2018–20Two Form 483s, at Birmingham, Alabama.
  2. 2020The longest 483 on file: 7 observations over 3 pages at Birmingham, Alabama.
  3. 2024One Form 483, at Birmingham, Alabama.

Cited most

Across all Evonik observations on file

The complete Evonik 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
2024-12-10483 Form 483$99
2020-01-10483 Form 483$99
2018-08-10483 Form 483$99

Investigators on these documents

Camerson E. Moore (1)Claire M. Minden (1)

FEI number 3012757951 · most recent document Dec 10, 2024

About Evonik Corporation

How many FDA Form 483s has Evonik Corporation received?

FDA Intel has 3 Form 483s on file for Evonik Corporation; the most recent is dated Dec 10, 2024.

When was Evonik Corporation last inspected by FDA?

The most recent FDA inspection document on file for Evonik Corporation is a Form 483 dated Dec 10, 2024, for the site in Birmingham, Alabama.

What did FDA cite at Evonik Corporation?

The regulations cited most in the observations on file for Evonik Corporation are 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 4 times; 21 CFR 211.113 (Control of microbiological contamination), 3 times; 21 CFR 211.160 (General requirements), 2 times.