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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 January 25, 2019 in Northridge, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

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

Facility

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  • 1151074 (NAI Wed Jul 28 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1077108 (VAI Fri Jan 25 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1008836 (VAI Mon Mar 06 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 940328 (VAI Tue Sep 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources