# FDA Inspection 780633 - MDF Instruments Direct, Inc. - May 03, 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 for MDF Instruments Direct, Inc. on May 03, 2012. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 780633 - 2012-05-03](https://www.keypedia.com/records/fda_inspections/mdf-instruments-direct-inc/592cb152-306c-4b6c-819c-81b8a8f1f907)

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