# FDA Inspection 1058782 - DuoProSS Meditech Corporation - July 13, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/duopross-meditech-corporation/da92356f-2b64-4125-9700-ed9c4fa732fb
Source feed: FDA_Inspections

> FDA Inspection 1058782 for DuoProSS Meditech Corporation on July 13, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1058782
- Company Name: DuoProSS Meditech Corporation
- Inspection Date: 2018-07-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/duopross-meditech-corporation/e2b0e029-08e4-4e03-80a8-c60e7098bfcc

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