# FDA Inspection 1177939 - GETSCH+HILLER MEDIZINTECHNIK GmbH - July 21, 2022

Source: https://www.keypedia.com/records/fda_inspections/getschhiller-medizintechnik-gmbh/271939d9-40f6-4528-afed-0464adb8d530
Source feed: FDA_Inspections

> FDA Inspection 1177939 for GETSCH+HILLER MEDIZINTECHNIK GmbH on July 21, 2022. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1177939
- Company Name: GETSCH+HILLER MEDIZINTECHNIK GmbH
- Inspection Date: 2022-07-21
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1177939 - 2022-07-21](https://www.keypedia.com/records/fda_inspections/getschhiller-medizintechnik-gmbh/e1780dc1-824e-4035-b74a-5aa3fdedde88)
- [FDA Inspection 1097883 - 2019-06-06](https://www.keypedia.com/records/fda_inspections/getschhiller-medizintechnik-gmbh/cb6e3a0c-27e0-4bea-accf-193e19a92cac)
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Company: https://www.keypedia.com/companies/getschhiller-medizintechnik-gmbh/d572824c-30a5-4118-8d56-9c354287bcc0

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