FDA Inspection 1030008 — Unimark Remedies Limited

Unimark Remedies Limited — FEI 3004414652

The FDA completed an inspection of Unimark Remedies Limited on September 29, 2017 in Vapi. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 29, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Vapi (India)