FDA Inspection 982337 — Kindeva Drug Delivery Limited

Kindeva Drug Delivery Limited — FEI 3002807586

The FDA completed an inspection of Kindeva Drug Delivery Limited on Aug 12, 2016 in Loughborough. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 12, 2016
Fiscal Year
2016
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.