# FDA Inspection 960833 - PRO-TECH Design & Mfg., Inc. - February 29, 2016

Source: https://www.keypedia.com/records/fda_inspections/pro-tech-design-mfg-inc/9154cbbb-551a-4f93-b0ea-7ee976ba53d2
Source feed: FDA_Inspections

> FDA Inspection 960833 for PRO-TECH Design & Mfg., Inc. on February 29, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 960833
- Company Name: PRO-TECH Design & Mfg., Inc.
- Inspection Date: 2016-02-29
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/pro-tech-design-mfg-inc/f84ae588-49bd-4504-af30-a1818fd1927e

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