# FDA Inspection 1002898 - Duralife-USA, LLC - February 07, 2017

Source: https://www.keypedia.com/records/fda_inspections/duralife-usa-llc/559362e1-c374-4e9a-956c-1725474e5797
Source feed: FDA_Inspections

> FDA Inspection 1002898 for Duralife-USA, LLC on February 07, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1002898
- Company Name: Duralife-USA, LLC
- Inspection Date: 2017-02-07
- 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/duralife-usa-llc/1338c2d2-4731-4389-b29d-dc172479caca

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