FDA Inspection 1202201 — Kindeva Drug Delivery Limited

Kindeva Drug Delivery Limited — FEI 3002807586

The FDA completed an inspection of Kindeva Drug Delivery Limited on May 27, 2021 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
May 27, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Loughborough (United Kingdom)

Additional Details

Mutual Recognition Agreement (MRA)