# FDA Inspection 600292 - Merete GmbH - July 02, 2009

Source: https://www.keypedia.com/records/fda_inspections/merete-gmbh/ca972514-bfb4-4852-9d63-215cb0ea3bd5
Source feed: FDA_Inspections

> FDA Inspection 600292 for Merete GmbH on July 02, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 600292
- Company Name: Merete GmbH
- Inspection Date: 2009-07-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 600292 - 2009-07-02](https://www.keypedia.com/records/fda_inspections/merete-gmbh/58ac488c-35b4-4dfd-8dc6-8a5453f5b401)

Company: https://www.keypedia.com/companies/merete-gmbh/756e1255-3cc0-4585-8a62-bb869e1e9b8b

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