FDA Inspection 1254538 — Dyno Manufacturing, Inc.

Dyno Manufacturing, Inc. — FEI 3017219182

The FDA completed an inspection of Dyno Manufacturing, Inc. on November 1, 2024 in Madison, IL. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
November 1, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Madison, IL (United States)