# FDA Inspection 638362 - Durasafe Inc - November 24, 2009

Source: https://www.keypedia.com/records/fda_inspections/durasafe-inc/8e12dfb2-8d06-4c45-9528-04387a5147c4
Source feed: FDA_Inspections

> FDA Inspection 638362 for Durasafe Inc on November 24, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 638362
- Company Name: Durasafe Inc
- Inspection Date: 2009-11-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/durasafe-inc/828904a3-9835-4d21-886e-f6c6cb59497d

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