Max Plus Laser Co. Ltd. – FDA Inspection, May 25, 2017

Record Details

This FDA Inspection record concerns Max Plus Laser Co. Ltd., with an inspection on May 25, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Max Plus Laser Co. Ltd.
Inspection Date: May 25, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health
People: Andre S. Lamontagne (Issuing Officer)
Emir Galevi (Issuing Officer)

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ID · cdd7dbaf-fcdf-4dd8-bc4e-02714505ab4c

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number: 1068987
FDA center: Medical Devices & Rad Health
Project area: Radiation Control and Health Safety Act

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FDA Inspection

Max Plus Laser Co. Ltd.May 25, 2017