FDA Inspection 922069 — Kindeva Drug Delivery Limited

Kindeva Drug Delivery Limited — FEI 3002807586

The FDA completed an inspection of Kindeva Drug Delivery Limited on Mar 5, 2015 in Loughborough. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Mar 5, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Loughborough (United Kingdom)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.