# Ermis MedTech GmbH – FDA Inspection, Jun 12, 2024

Source: https://www.keypedia.com/records/fda_inspections/ermis-medtech-gmbh/e483ab7b-7ac0-4f2d-8bed-9b705b91a277
Source feed: FDA_Inspections

> FDA inspection 1243750 of Ermis MedTech GmbH, June 12, 2024. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1243750
- Company Name: Ermis MedTech GmbH
- Inspection Date: 2024-06-12
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1102918 - 2019-08-29

## Related Officers

- [Melanie W. Pishnery](https://www.keypedia.com/people/melanie-w-pishnery/ff4846b0-ffe1-4df0-9116-4bb238866b3a)

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