Roquette America, Inc.

FDA inspection history in Keokuk, Iowa, 2021 to 2026

2
Form 483s

Every document, by year

  • Form 483

2021: one Form 483; 2026: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2021One Form 483, at Keokuk, Iowa.
  2. 2026One Form 483, at Keokuk, Iowa.
  3. 2026The longest 483 on file: 3 observations over 3 pages at Keokuk, Iowa.

Cited most

Across all Roquette America observations on file

The complete Roquette America 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
2026-01-30483 Form 483$99
2021-06-17483 Form 483$99

FEI number 1910565 · most recent document Jan 30, 2026

About Roquette America, Inc.

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

FDA Intel has 2 Form 483s on file for Roquette America, Inc.; the most recent is dated Jan 30, 2026.

When was Roquette America, Inc. last inspected by FDA?

The most recent FDA inspection document on file for Roquette America, Inc. is a Form 483 dated Jan 30, 2026, for the site in Keokuk, Iowa.

What did FDA cite at Roquette America, Inc.?

The regulations cited most in the observations on file for Roquette America, Inc. are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.166 (Stability testing), 1 time; 21 CFR 211.192 (Production record review), 1 time.