# FDA Inspection 884754 - Promedtek, Inc. - June 26, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/promedtek-inc/55a33e1b-d88a-4637-8029-39d9e145f15a
Source feed: FDA_Inspections

> FDA Inspection 884754 for Promedtek, Inc. on June 26, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 884754
- Company Name: Promedtek, Inc.
- Inspection Date: 2014-06-26
- 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.globalkeysolutions.net/companies/promedtek-inc/1c53d2ae-12c9-4971-becf-37e1f801ed6e

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