# Martech Medical Products, Mexico – FDA Inspection, Sep 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/martech-medical-products-mexico/9f14d5b8-dff1-4769-9726-e47cb07ca98d
Source feed: FDA_Inspections

> FDA inspection 1027644 of Martech Medical Products, Mexico, September 28, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1027644
- Company Name: Martech Medical Products, Mexico
- Inspection Date: 2017-09-28
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/kyle-j-mccracken/5085937f-3231-4639-8d84-0e528a954824)
- [Company Rep](https://www.keypedia.com/people/susan-m-matthias/cd23c465-4411-4988-8676-2089e265622a)

Company: https://www.keypedia.com/companies/martech-medical-products-mexico/76e77ddd-b31a-4fb9-b1ff-37e95fcff0a3

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