FDA Inspection 985558 — WHITMAN LABORATORIES LTD.
The FDA completed an inspection of WHITMAN LABORATORIES LTD. on August 5, 2016 in Petersfield. 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
- August 5, 2016
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Petersfield (United Kingdom)