Centaur, Inc.

FDA inspection history in Olathe, Kansas, 2010 to 2024

1
Form 483
1
Warning letter

Every document, by year

  • Form 483
  • Warning letter

2010: one warning letter; 2024: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2010One warning letter, at Olathe, Kansas.
  2. 2024One Form 483, at Olathe, Kansas.

Cited most

Across all Centaur observations on file

The complete Centaur 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
2024-02-01483 Form 483$99
2010-01-08Warning letter Warning letter$99

Investigators on these documents

Conner N. Mann (1)

FEI number 1931750 · most recent document Feb 1, 2024

About Centaur, Inc.

How many FDA Form 483s has Centaur, Inc. received?

FDA Intel has 1 Form 483 on file for Centaur, Inc.; the most recent is dated Feb 1, 2024.

When was Centaur, Inc. last inspected by FDA?

The most recent FDA inspection document on file for Centaur, Inc. is a Form 483 dated Feb 1, 2024, for the site in Olathe, Kansas.

What did FDA cite at Centaur, Inc.?

The regulations cited most in the observations on file for Centaur, Inc. are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.80(a) (General requirements), 1 time.

Has Centaur, Inc. received an FDA warning letter?

Yes. FDA Intel has 1 FDA warning letter on file for Centaur, Inc.; the most recent is dated Jan 8, 2010.