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FDA Inspection
•VectraCor, Inc•September 27, 2017

VectraCor, Inc – FDA Inspection, Sep 27, 2017

Record Details

This FDA Inspection record concerns VectraCor, Inc, with an inspection on September 27, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
VectraCor, Inc
Inspection Date
September 27, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Melissa A. Zuppe
View Company Profile

ID · 6d38ca9d-e879-4252-afad-7fe26abd0668

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1026740
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 820.198(e)Records of complaint investigation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of VectraCor, Inc

1
DateClassificationOfficeProject area
November 6, 2012VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for VectraCor, Inc
  • FDA Inspection 808583 - 2012-11-06

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