# FDA Inspection 713600 - Heidelberg Engineering GmbH - February 03, 2011

Source: https://www.keypedia.com/records/fda_inspections/heidelberg-engineering-gmbh/59e8f82a-e4c9-4275-b39a-4f8709bd6f9f
Source feed: FDA_Inspections

> FDA Inspection 713600 for Heidelberg Engineering GmbH on February 03, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 713600
- Company Name: Heidelberg Engineering GmbH
- Inspection Date: 2011-02-03
- 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/heidelberg-engineering-gmbh/efbbd335-8882-4179-8a90-d4d165e802f0

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