# CoreLink LLC – FDA Inspection, Feb 4, 2013

Source: https://www.keypedia.com/records/fda_inspections/corelink-llc/0ff121d5-a567-4c96-bc06-f5f1ee362050
Source feed: FDA_Inspections

> FDA inspection 818928 of CoreLink LLC, February 04, 2013. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 818928
- Company Name: CoreLink LLC
- Inspection Date: 2013-02-04
- 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: 3

## Related Documents

- FDA Inspection 1176784 - 2022-07-27
- FDA Inspection 1019655 - 2017-07-21
- FDA Inspection 933648 - 2015-07-09
- FDA Inspection 698189 - 2010-11-12

Company: https://www.keypedia.com/companies/corelink-llc/c85f28dc-c207-4608-861e-4382e9ab21f9

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