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FDA Inspection
•Augmenix Inc•May 22, 2019

Augmenix Inc – FDA Inspection, May 22, 2019

Record Details

This FDA Inspection record concerns Augmenix Inc, with an inspection on May 22, 2019, issued by the New England District Office, covering medical devices & rad health.

Company
Augmenix Inc
Inspection Date
May 22, 2019
Product Type
Medical Devices & Rad Health
Office
New England District Office
View Company Profile

ID · 8ff429ba-7511-46f0-acd0-ef2824338c3a

Inspection Facts

Inspection number
1159303
FDA center
Medical Devices & Rad Health
Outcome
Form 483 issued

Other FDA inspections of Augmenix Inc

2
DateClassificationOfficeProject area
October 17, 2014VAICenter for Devices and Radiological HealthCompliance: Devices
January 12, 2012NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Augmenix Inc
  • FDA Inspection 901350 - 2014-10-17
  • FDA Inspection 762778 - 2012-01-12

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