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FDA Inspection
•Sagemax Bioceramics, Inc.•October 13, 2017

Sagemax Bioceramics, Inc. – FDA Inspection, Oct 13, 2017

Record Details

This FDA Inspection record concerns Sagemax Bioceramics, Inc., with an inspection on October 13, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Sagemax Bioceramics, Inc.
Inspection Date
October 13, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Stephen R. Souza (Investigator)
View Company Profile

ID · 6409b3ac-d8ee-438c-bd7e-8d6d3dc52844

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1030254
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Sagemax Bioceramics, Inc.

4
DateClassificationOfficeProject area
June 3, 2015VAICenter for Devices and Radiological HealthCompliance: Devices
August 18, 2014OAICenter for Devices and Radiological HealthCompliance: Devices
January 24, 2012NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
July 2, 2010VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Sagemax Bioceramics, Inc.
  • FDA Inspection 930078 - 2015-06-03
  • FDA Inspection 892877 - 2014-08-18
  • FDA Inspection 766593 - 2012-01-24
  • FDA Inspection 672024 - 2010-07-02

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