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FDA Inspection
•VPDiagnostics Inc•January 18, 2017

VPDiagnostics Inc – FDA Inspection, Jan 18, 2017

Record Details

This FDA Inspection record concerns VPDiagnostics Inc, with an inspection on January 18, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
VPDiagnostics Inc
Inspection Date
January 18, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Stephen R. Souza (Investigator)
View Company Profile

ID · fd694c0c-ce4f-4bbb-b227-aa9cd9a1e344

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
999133
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 820.22Quality audits - Lack of or inadequate procedures
  2. 21 CFR 820.40Procedures not adequately established or maintained

Full citation text and observation details available on the Dashboard.

Other FDA inspections of VPDiagnostics Inc

2
DateClassificationOfficeProject area
November 8, 2013NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
October 18, 2011VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for VPDiagnostics Inc
  • FDA Inspection 854707 - 2013-11-08
  • FDA Inspection 749836 - 2011-10-18

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