# MDF Instruments Direct, Inc. – FDA Inspection, May 3, 2012

Source: https://www.keypedia.com/records/fda_inspections/mdf-instruments-direct-inc/b37b88cf-32fa-43d3-9f1c-31cc1df4fdfd
Source feed: FDA_Inspections

> FDA inspection 780633 of MDF Instruments Direct, Inc., May 03, 2012. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 803.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 780633
- Company Name: MDF Instruments Direct, Inc.
- Inspection Date: 2012-05-03
- 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: 1

Company: https://www.keypedia.com/companies/mdf-instruments-direct-inc/843ca757-8798-415b-8d88-1d957ef10420

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