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FDA Inspection
•Planmeca Oy•August 18, 2017

Planmeca Oy – FDA Inspection, Aug 18, 2017

Record Details

This FDA Inspection record concerns Planmeca Oy, with an inspection on August 18, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.

Company
Planmeca Oy
Inspection Date
August 18, 2017
Product Type
Medical Devices & Rad Health
Office
Office of Inspections and Investigations
Person
  • Yehualashet A. Gessesse (Company Rep)
View Company Profile

ID · 844011cf-c49c-4c57-8687-7c1259b68d85

Inspection Facts

Inspection number
1028452
FDA center
Medical Devices & Rad Health
Outcome
Form 483 issued

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