# FDA Inspection 808378 - Precision Interconnect, LLC - November 13, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/precision-interconnect-llc/fbe8697e-a935-48f7-b21a-e35e10eed9ee
Source feed: FDA_Inspections

> FDA Inspection 808378 for Precision Interconnect, LLC on November 13, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 808378
- Company Name: Precision Interconnect, LLC
- Inspection Date: 2012-11-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 986629 - 2016-09-19](https://www.globalkeysolutions.net/records/fda_inspections/precision-interconnect-llc/cb501b71-ccd4-4190-8070-24246dff0dda)
- [FDA Inspection 986629 - 2016-09-19](https://www.globalkeysolutions.net/records/fda_inspections/precision-interconnect-llc/77e3d3bb-e7e5-4ab0-ab8b-7e42141fae49)
- [FDA Inspection 808378 - 2012-11-13](https://www.globalkeysolutions.net/records/fda_inspections/precision-interconnect-llc/03287e26-85da-445e-ac82-f13787aa3fc9)

Company: https://www.globalkeysolutions.net/companies/precision-interconnect-llc/48ca24b9-175a-4447-be0c-af45a15c4e75

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