FDA Inspection 628411 — Nipro Medical Industries, Ltd.

Nipro Medical Industries, Ltd. — FEI 3002807725

The FDA completed an inspection of Nipro Medical Industries, Ltd. on Nov 17, 2009 in Tatebayashi. 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). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 17, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Tatebayashi (Japan)

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