# RM Temena GmbH – FDA Inspection, Feb 27, 2014

Source: https://www.keypedia.com/records/fda_inspections/rm-temena-gmbh/f1313d8f-70c6-41fb-aa36-4b2241d82601
Source feed: FDA_Inspections

> FDA inspection 871224 of RM Temena GmbH, February 27, 2014. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 871224
- Company Name: RM Temena GmbH
- Inspection Date: 2014-02-27
- 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

Company: https://www.keypedia.com/companies/rm-temena-gmbh/170d3de7-232d-45cb-acbc-32bd723f6cfb

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