FDA Inspection 1077108 — Kindeva Drug Delivery L.P.

Kindeva Drug Delivery L.P. — FEI 2010441

The FDA completed an inspection of Kindeva Drug Delivery L.P. on January 25, 2019 in Northridge, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 25, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Northridge, CA (United States)

Citations

IDCFRDescription
110521 CFR 211.22(d)Procedures not in writing, fully followed
189121 CFR 211.165(f)Failing drug products not rejected