# Sirtex Wilmington LLC – FDA Inspection, Jul 10, 2025

Source: https://www.keypedia.com/records/fda_inspections/sirtex-wilmington-llc/275bcb44-42ed-4485-a7c2-b73b4e53d386
Source feed: FDA_Inspections

> FDA inspection 1267696 of Sirtex Wilmington LLC, July 10, 2025. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1267696
- Company Name: Sirtex Wilmington LLC
- Inspection Date: 2025-07-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: New England District Office
- Citation Count: 6

## Related Documents

- [FDA Inspection 840306 - 2013-07-12](https://www.keypedia.com/records/fda_inspections/sirtex-wilmington-llc/8d76d4d7-0bda-4ea4-a725-7c34d36c36d6)
- FDA Inspection 723153 - 2011-05-10
- [FDA Inspection 578579 - 2009-01-30](https://www.keypedia.com/records/fda_inspections/sirtex-wilmington-llc/62c043b0-3fba-4705-b16a-f6758b4f14de)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/sunita-pandey/008e5bb8-0eb3-45d8-8524-734ac0454250)

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

Office: https://www.keypedia.com/offices/new-england-district-office/aa458072-2f1d-4231-89f5-21ba7a3b7144