# FDA Inspection 1009746 - Promedtek, Inc. - April 06, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/promedtek-inc/f7fc024c-46fc-4c1c-a37c-46a9fc9436a5/
Source feed: FDA_Inspections

> FDA Inspection 1009746 for Promedtek, Inc. on April 06, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1009746
- Company Name: Promedtek, Inc.
- Inspection Date: 2017-04-06
- Classification: Voluntary Action Indicated (VAI)
- 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