# FABRITEQ LLC – FDA Inspection, Nov 1, 2017

Source: https://www.keypedia.com/records/fda_inspections/fabriteq-llc/b7262890-be04-425c-bb4e-09f8c5fcae30
Source feed: FDA_Inspections

> FDA inspection 1031306 of FABRITEQ LLC, November 01, 2017. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031306
- Company Name: FABRITEQ LLC
- Inspection Date: 2017-11-01
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1174991 - 2022-06-14

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/fabriteq-llc/1389a7e4-3c99-46e6-84b5-be7819b438e2

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