FDA Inspection 1061585 — Kindeva Drug Delivery Limited

Kindeva Drug Delivery Limited — FEI 3002807586

The FDA completed an inspection of Kindeva Drug Delivery Limited on Jun 30, 2017 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
Jun 30, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Loughborough (United Kingdom)

Additional details

Mutual Recognition Agreement (MRA)

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