FDA Inspection 1019432 — TOLMAR, Inc.
The FDA completed an inspection of TOLMAR, Inc. on July 26, 2017 in Windsor, 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
- July 26, 2017
- Fiscal Year
- 2017
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Windsor, CO (United States)