# FDA Inspection 982059 - Devicor Medical Products Inc - August 01, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/devicor-medical-products-inc/dd74e3b7-ec75-47f0-9860-2a65bcb31bdd
Source feed: FDA_Inspections

> FDA Inspection 982059 for Devicor Medical Products Inc on August 01, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 982059
- Company Name: Devicor Medical Products Inc
- Inspection Date: 2016-08-01
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 982059 - 2016-08-01](https://www.globalkeysolutions.net/records/fda_inspections/devicor-medical-products-inc/26ba7572-b582-47ff-a9e8-d83c054ef83e)
- [FDA Inspection 814919 - 2013-01-14](https://www.globalkeysolutions.net/records/fda_inspections/devicor-medical-products-inc/c16b72f5-c3cf-476e-8f64-79821160950d)

Company: https://www.globalkeysolutions.net/companies/devicor-medical-products-inc/3fc83e4f-bda4-4175-b50f-c928b846a340

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