# Hans Rudolph Inc – FDA Inspection, Feb 22, 2017

Source: https://www.keypedia.com/records/fda_inspections/hans-rudolph-inc/885fcc1e-93ac-44bf-8c28-dbd62720bef0
Source feed: FDA_Inspections

> FDA inspection 1002408 of Hans Rudolph Inc, February 22, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1002408
- Company Name: Hans Rudolph Inc
- Inspection Date: 2017-02-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 853640 - 2013-10-07
- FDA Inspection 634965 - 2009-12-04

## Related Officers

- [Investigator](https://www.keypedia.com/people/eric-c-fox/218af117-1551-476f-80ba-172e2cd6baee)

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