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FDA Inspection
•Cardinal Health PR 218 Inc•November 16, 2016

Cardinal Health PR 218 Inc – FDA Inspection, Nov 16, 2016

Record Details

This FDA Inspection record concerns Cardinal Health PR 218 Inc, with an inspection on November 16, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company
Cardinal Health PR 218 Inc
Inspection Date
November 16, 2016
Product Type
Devices
Office
Center for Devices and Radiological Health
People
  • Adaliz Santaliz-Cruz (FDA Associated Person)
  • Maricelys Mercado (Company Rep)
View Company Profile

ID · f9dc7b34-3dd6-44fa-b5f9-1cea74addfe0

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
993501
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

Other FDA inspections of Cardinal Health PR 218 Inc

2
DateClassificationOfficeProject area
January 29, 2013VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
February 15, 2011NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Cardinal Health PR 218 Inc
  • FDA Inspection 817049 - 2013-01-29
  • FDA Inspection 710940 - 2011-02-15

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