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FDA Inspection
•FUSION ORTHOPEDICS USA•December 21, 2018

FUSION ORTHOPEDICS USA – FDA Inspection, Dec 21, 2018

Record Details

This FDA Inspection record concerns FUSION ORTHOPEDICS USA, with an inspection on December 21, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
FUSION ORTHOPEDICS USA
Inspection Date
December 21, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Charles L. Larson (Company Rep)
View Company Profile

ID · e7e1b0a6-5814-4efd-b34a-3a92b6f7492d

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1080822
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

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