# FDA Inspection 670941 - Andreas Hettich Gmbh & Co. Kg - June 17, 2010

Source: https://www.keypedia.com/records/fda_inspections/andreas-hettich-gmbh-co-kg/399b0a8f-3f5c-4e72-922a-e5074573b8d5
Source feed: FDA_Inspections

> FDA Inspection 670941 for Andreas Hettich Gmbh & Co. Kg on June 17, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 670941
- Company Name: Andreas Hettich Gmbh & Co. Kg
- Inspection Date: 2010-06-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 670941 - 2010-06-17](https://www.keypedia.com/records/fda_inspections/andreas-hettich-gmbh-co-kg/e95f400f-3458-4d6d-ba90-ce018960656a)

Company: https://www.keypedia.com/companies/andreas-hettich-gmbh-co-kg/822173c7-1dc7-4679-b65d-76d5846d99de

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