# Weidmann Plastics Technology AG – FDA Inspection, Mar 21, 2013

Source: https://www.keypedia.com/records/fda_inspections/weidmann-plastics-technology-ag/47626062-84ab-4bed-82e6-07642428541f
Source feed: FDA_Inspections

> FDA inspection 830064 of Weidmann Plastics Technology AG, March 21, 2013. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 830064
- Company Name: Weidmann Plastics Technology AG
- Inspection Date: 2013-03-21
- 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: 4

Company: https://www.keypedia.com/companies/weidmann-plastics-technology-ag/e7d58d0d-5cea-4268-bfca-c82cf75e4823

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