# FDA Inspection 1102918 - Ermis MedTech GmbH - August 29, 2019

Source: https://www.keypedia.com/records/fda_inspections/ermis-medtech-gmbh/19c4e5c8-77b1-4064-aa67-faa6923746cc
Source feed: FDA_Inspections

> FDA Inspection 1102918 for Ermis MedTech GmbH on August 29, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102918
- Company Name: Ermis MedTech GmbH
- Inspection Date: 2019-08-29
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/ermis-medtech-gmbh/1e5015c2-2a29-4569-a0af-3d55cf638cc4

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7