Dyno Manufacturing, Inc

FDA inspection history in Madison, Illinois, 2024 to 2025

1
Warning letter: 1
Form 483

Every document, by year

Warning letter
Form 483

The story so far

Built from the dates and citations on the documents themselves.

2024–25One Form 483 and one warning letter, at Madison, Illinois.

Cited most

Across all Dyno Manufacturing observations on file

21 CFR 211.100
Written procedures; deviations
1
21 CFR 211.166
Stability testing
1
21 CFR 211.180
General requirements
1
21 CFR 211.22
Responsibilities of quality control unit
1

The complete Dyno Manufacturing 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

Madison, Illinois
One warning letter and one Form 483 · 2024 to 2025 · 3 observations
Latest: Warning letter, Apr 9, 2025 →

Documents

2 on file, newest first

Date	Document	Location	Observations	Price
2025-04-09	Warning letter Warning letter	Madison, Illinois	—	$99
2024-11-01	483 Form 483	Madison, Illinois	3	$99

FEI number 3017219182 · most recent document Apr 9, 2025

About Dyno Manufacturing, Inc

How many FDA Form 483s has Dyno Manufacturing, Inc received?

FDA Intel has 1 Form 483 on file for Dyno Manufacturing, Inc; the most recent is dated Nov 1, 2024.

When was Dyno Manufacturing, Inc last inspected by FDA?

The most recent FDA inspection document on file for Dyno Manufacturing, Inc is a Form 483 dated Nov 1, 2024, for the site in Madison, Illinois.

What did FDA cite at Dyno Manufacturing, Inc?

The regulations cited most in the observations on file for Dyno Manufacturing, Inc are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.166 (Stability testing), 1 time; 21 CFR 211.180 (General requirements), 1 time.

Has Dyno Manufacturing, Inc received an FDA warning letter?

Yes. FDA Intel has 1 FDA warning letter on file for Dyno Manufacturing, Inc; the most recent is dated Apr 9, 2025.