# DuoProSS Meditech Corporation – FDA Inspection, Jul 13, 2018

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

> FDA inspection 1058782 of DuoProSS Meditech Corporation, July 13, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

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- [FDA Inspection 1177699 - 2022-08-12](https://www.keypedia.com/records/fda_inspections/duopross-meditech-corporation/866e9066-b04b-4816-bc56-52a088de1be7)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/kwong-p-lee/f4778925-1fad-4988-9e39-86482896c4fa)

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

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