# FDA Inspection 885787 - Precept Medical Products Inc - June 20, 2014

Source: https://www.keypedia.com/records/fda_inspections/precept-medical-products-inc/1fb11cb1-8a79-465a-a594-19e632806f5e
Source feed: FDA_Inspections

> FDA Inspection 885787 for Precept Medical Products Inc on June 20, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 885787
- Company Name: Precept Medical Products Inc
- Inspection Date: 2014-06-20
- 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/precept-medical-products-inc/b7a0a6cb-ff27-4a78-9c8a-3c5f6cb73ae2

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