# FDA Inspection 984229 - Quintron Instrument Co Inc - March 02, 2016

Source: https://www.keypedia.com/records/fda_inspections/quintron-instrument-co-inc/cefa10d6-3979-43ac-b48b-3a9bf33f0ecd
Source feed: FDA_Inspections

> FDA Inspection 984229 for Quintron Instrument Co Inc on March 02, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 984229
- Company Name: Quintron Instrument Co Inc
- Inspection Date: 2016-03-02
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/quintron-instrument-co-inc/85029207-e1a9-407d-8690-899ca32d7259

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