FDA Warning Letter — Dyno Manufacturing, Inc.

Case 700785 — FEI 3017219182

The FDA took a Warning Letter action against Dyno Manufacturing, Inc. on April 15, 2025 (Madison, IL). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Dyno Manufacturing, Inc.
Date
April 15, 2025
Fiscal Year
2025
Product Type
Drugs
Center
CDER
Location
Madison, IL (United States)