# FDA Inspection 696342 - Providien Device Assembly, LLC - November 03, 2010

Source: https://www.keypedia.com/records/fda_inspections/providien-device-assembly-llc/d16b4f31-7ff0-48eb-82e9-ffa9b04e483b
Source feed: FDA_Inspections

> FDA Inspection 696342 for Providien Device Assembly, LLC on November 03, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 696342
- Company Name: Providien Device Assembly, LLC
- Inspection Date: 2010-11-03
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 781067 - 2012-05-04](https://www.keypedia.com/records/fda_inspections/providien-device-assembly-llc/f9fff157-7d09-410f-8b84-046cfc5412af)

Company: https://www.keypedia.com/companies/providien-device-assembly-llc/10478c1d-19e7-4527-93cc-71dc06033b1f

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