FDA Inspection 829337 — Vitalife Laboratories (A Div. Of Arch Pharmalabs Limited)
The FDA completed an inspection of Vitalife Laboratories (A Div. Of Arch Pharmalabs Limited) on April 12, 2013 in Gurugram. 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 12, 2013
- Fiscal Year
- 2013
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Gurugram (India)