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FDA Inspection
•Nipro Medical Industries, Ltd.•November 15, 2018

Nipro Medical Industries, Ltd. – FDA Inspection, Nov 15, 2018

Record Details

This FDA Inspection record concerns Nipro Medical Industries, Ltd., with an inspection on November 15, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
Nipro Medical Industries, Ltd.
Inspection Date
November 15, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Juanita Banuelos (Company Rep)
View Company Profile

ID · e06dc344-8001-42e6-b5d1-673e5603a4ec

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1079443
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

Other FDA inspections of Nipro Medical Industries, Ltd.

3
DateClassificationOfficeProject area
May 15, 2013NAICenter for Devices and Radiological HealthCompliance: Devices
September 22, 2011NAICenter for Devices and Radiological HealthCompliance: Devices
November 17, 2009VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Nipro Medical Industries, Ltd.
  • FDA Inspection 834550 - 2013-05-15
  • FDA Inspection 748648 - 2011-09-22
  • FDA Inspection 628411 - 2009-11-17

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