ABS Corporation

FDA inspection history in Omaha, Nebraska, 2023 to 2026

1
Warning letter
1
Form 483

Every document, by year

  • Warning letter
  • Form 483

2023: one Form 483; 2026: one warning letter.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2023One Form 483, at Omaha, Nebraska.
  2. 2026One warning letter, at Omaha, Nebraska.

Cited most

Across all ABS observations on file

The complete ABS 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
2026-07-23Warning letter Warning letter$99
2023-08-11483 Form 483$99

Investigators on these documents

Torrey M. Ward (1)

FEI number 1950042 · most recent document Jul 23, 2026

About ABS Corporation

How many FDA Form 483s has ABS Corporation received?

FDA Intel has 1 Form 483 on file for ABS Corporation; the most recent is dated Aug 11, 2023.

When was ABS Corporation last inspected by FDA?

The most recent FDA inspection document on file for ABS Corporation is a Form 483 dated Aug 11, 2023, for the site in Omaha, Nebraska.

What did FDA cite at ABS Corporation?

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

Has ABS Corporation received an FDA warning letter?

Yes. FDA Intel has 1 FDA warning letter on file for ABS Corporation; the most recent is dated Jul 23, 2026.