FDA Inspection 713719 — Morepen Laboratories Limited

Morepen Laboratories Limited — FEI 3002807612

The FDA completed an inspection of Morepen Laboratories Limited on October 14, 2010 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
October 14, 2010
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Solan (India)