# Duralife-USA, LLC – FDA Inspection, Feb 7, 2017

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

> FDA inspection 1002898 of Duralife-USA, LLC, February 07, 2017. Classification: Voluntary Action Indicated (VAI). 10 citations under 21 CFR parts 803 and 820. Form 483 issued.

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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)
- 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: 10

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/brandi-l-garbutt/6e28acd2-040b-49d4-8589-999321bbadb6)

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