FDA Inspection 1040453 — Asahi Intecc USA, Inc.

Asahi Intecc USA, Inc. — FEI 3013854616

The FDA completed an inspection of Asahi Intecc USA, Inc. on Jan 25, 2018 in Santa Ana, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 25, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Santa Ana, CA (United States)

Additional Details

Sponsor, Contract Research Organization

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