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FDA Inspection
•Ermis MedTech GmbH•June 12, 2024

Ermis MedTech GmbH – FDA Inspection, Jun 12, 2024

Record Details

This FDA Inspection record concerns Ermis MedTech GmbH, with an inspection on June 12, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company
Ermis MedTech GmbH
Inspection Date
June 12, 2024
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Melanie W. Pishnery
View Company Profile

ID · e483ab7b-7ac0-4f2d-8bed-9b705b91a277

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1243750
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Ermis MedTech GmbH

1
DateClassificationOfficeProject area
August 29, 2019NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Ermis MedTech GmbH
  • FDA Inspection 1102918 - 2019-08-29

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