# FDA Inspection 916389 - Newmatic Inc. - March 03, 2015

Source: https://www.keypedia.com/records/fda_inspections/newmatic-inc/41cea065-457d-4e00-bf0a-1d1c8435f1f1
Source feed: FDA_Inspections

> FDA Inspection 916389 for Newmatic Inc. on March 03, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 916389
- Company Name: Newmatic Inc.
- Inspection Date: 2015-03-03
- 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/newmatic-inc/2001931f-be2c-4f15-bf03-a6d5b8a65f5d

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