# FDA Inspection 565629 - Xylos Corporation - September 30, 2009

Source: https://www.keypedia.com/records/fda_inspections/xylos-corporation/b7600a5f-e1fe-4bba-8fd2-0f1172472627
Source feed: FDA_Inspections

> FDA Inspection 565629 for Xylos Corporation on September 30, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 565629
- Company Name: Xylos Corporation
- Inspection Date: 2009-09-30
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/xylos-corporation/5d8d2579-01e7-41db-b40b-e22f7582fe17

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