FDA Inspection 883509 — Tolmar, Inc.

Tolmar, Inc. — FEI 3006218434

The FDA completed an inspection of Tolmar, Inc. on February 16, 2014 in Fort Collins, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 16, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Fort Collins, CO (United States)