# Markus Thalmann – FDA Inspection, Oct 10, 2013

Source: https://www.keypedia.com/records/fda_inspections/markus-thalmann/85097a07-4e5c-467c-9440-eac50913e61e
Source feed: FDA_Inspections

> FDA inspection 851365 of Markus Thalmann, October 10, 2013. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 851365
- Company Name: Markus Thalmann
- Inspection Date: 2013-10-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

Company: https://www.keypedia.com/companies/markus-thalmann/e7329968-f9ab-426b-b00f-5ec071dcd8b5

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