# Sirtex Wilmington LLC – FDA Inspection, Jul 12, 2013

Source: https://www.keypedia.com/records/fda_inspections/sirtex-wilmington-llc/8d76d4d7-0bda-4ea4-a725-7c34d36c36d6
Source feed: FDA_Inspections

> FDA inspection 840306 of Sirtex Wilmington LLC, July 12, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 840306
- Company Name: Sirtex Wilmington LLC
- Inspection Date: 2013-07-12
- 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

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Company: https://www.keypedia.com/companies/sirtex-wilmington-llc/6a8f8d3b-3634-4b89-9e79-17447bfbfd29

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