# FDA Inspection 634965 - Hans Rudolph Inc - December 04, 2009

Source: https://www.keypedia.com/records/fda_inspections/hans-rudolph-inc/15748900-40fe-4bcd-a4f0-d6d95274a11d
Source feed: FDA_Inspections

> FDA Inspection 634965 for Hans Rudolph Inc on December 04, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 634965
- Company Name: Hans Rudolph Inc
- Inspection Date: 2009-12-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/hans-rudolph-inc/d551197e-a331-416c-a659-54e657d4e479

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