FDA Inspection 827149 — Kindeva Drug Delivery Limited

Kindeva Drug Delivery Limited — FEI 3002807586

The FDA completed an inspection of Kindeva Drug Delivery Limited on April 15, 2013 in Loughborough. 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 15, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Loughborough (United Kingdom)