# FDA Inspection 860960 - Protech Professional Products, Inc. - December 13, 2013

Source: https://www.keypedia.com/records/fda_inspections/protech-professional-products-inc/f0cd407f-05c6-4e71-a8fc-db9508528246
Source feed: FDA_Inspections

> FDA Inspection 860960 for Protech Professional Products, Inc. on December 13, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 860960
- Company Name: Protech Professional Products, Inc.
- Inspection Date: 2013-12-13
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/protech-professional-products-inc/7a4ac453-00b3-4550-9bec-3a9d9885182f

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