FDA Inspection 1170739 — Omya, Inc

Omya, Inc — FEI 3003624292

The FDA completed an inspection of Omya, Inc on May 27, 2022 in Superior, AZ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 27, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Superior, AZ (United States)