# FDA Inspection 1098118 - Peramed Medizintechnik - July 25, 2019

Source: https://www.keypedia.com/records/fda_inspections/peramed-medizintechnik/0852b794-97e5-4ec3-a133-7882a0d60c3b
Source feed: FDA_Inspections

> FDA Inspection 1098118 for Peramed Medizintechnik on July 25, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1098118
- Company Name: Peramed Medizintechnik
- Inspection Date: 2019-07-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/peramed-medizintechnik/462f1073-bc87-4133-b9dd-761fe0291b35

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