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 Jan 25, 2019 in Northridge, CA. 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). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 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

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