# Rudolf Riester Gmbh – FDA Inspection, Jun 24, 2010

Source: https://www.keypedia.com/records/fda_inspections/rudolf-riester-gmbh/f21bf988-64cd-41fa-a29e-94ce36f8f8c3
Source feed: FDA_Inspections

> FDA inspection 672689 of Rudolf Riester Gmbh, June 24, 2010. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 672689
- Company Name: Rudolf Riester Gmbh
- Inspection Date: 2010-06-24
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 1101224 - 2019-05-16

Company: https://www.keypedia.com/companies/rudolf-riester-gmbh/d13f087e-2c75-4c3f-b02c-a800bc373843

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