FDA Inspection 1082205 — 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 NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 25, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Northridge, CA (United States)

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