FDA Inspection 615940 — Omya, Inc

Omya, Inc — FEI 3003624292

The FDA completed an inspection of Omya, Inc on Sep 9, 2009 in Superior, AZ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 9, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Superior, AZ (United States)