FDA Inspection 937997 — Morepen Laboratories Limited

Morepen Laboratories Limited — FEI 3002807612

The FDA completed an inspection of Morepen Laboratories Limited on April 17, 2015 in Solan. 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 17, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Solan (India)