FDA Inspection 1008836 — Kindeva Drug Delivery L.P.

Kindeva Drug Delivery L.P. — FEI 2010441

The FDA completed an inspection of Kindeva Drug Delivery L.P. on March 6, 2017 in Northridge, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 6, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Northridge, CA (United States)

Citations

IDCFRDescription
360321 CFR 211.160(b)Scientifically sound laboratory controls