FDA Inspection 1056151 — Tolmar, Inc.
The FDA completed an inspection of Tolmar, Inc. on April 6, 2018 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
- April 6, 2018
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Fort Collins, CO (United States)
Additional Details
Postmarket Adverse Drug Experience (PADE)