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FDA Inspection
•Aurora Spine Inc•May 23, 2014

Aurora Spine Inc – FDA Inspection, May 23, 2014

Record Details

This FDA Inspection record concerns Aurora Spine Inc, with an inspection on May 23, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company
Aurora Spine Inc
Inspection Date
May 23, 2014
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · ca9fb7e5-62ff-44fa-832c-0b4830e2dada

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
881967
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Aurora Spine Inc

2
DateClassificationOfficeProject area
July 30, 2018NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
September 18, 2017VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Aurora Spine Inc
  • FDA Inspection 1063919 - 2018-07-30
  • FDA Inspection 1028588 - 2017-09-18

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