FDA Inspection 1238561 — NIPRO CORP.

NIPRO CORP. — FEI 3002807710

The FDA completed an inspection of NIPRO CORP. on April 24, 2024 in Odate. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 24, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Odate (Japan)