# FDA Inspection 853640 - Hans Rudolph Inc - October 07, 2013

Source: https://www.keypedia.com/records/fda_inspections/hans-rudolph-inc/8299bc2b-94b4-4e6c-86bd-65f90da398a0
Source feed: FDA_Inspections

> FDA Inspection 853640 for Hans Rudolph Inc on October 07, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 853640
- Company Name: Hans Rudolph Inc
- Inspection Date: 2013-10-07
- Classification: No Action Indicated (NAI)
- 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