# MDF Instrumnets Medifriend Inc – FDA Inspection, Mar 27, 2009

Source: https://www.keypedia.com/records/fda_inspections/mdf-instrumnets-medifriend-inc/2294a4ef-0afd-484c-8a39-931ccbbfb819
Source feed: FDA_Inspections

> FDA inspection 586600 of MDF Instrumnets Medifriend Inc, March 27, 2009. Classification: Voluntary Action Indicated (VAI). 13 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 586600
- Company Name: MDF Instrumnets Medifriend Inc
- Inspection Date: 2009-03-27
- 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: 13

## Related Documents

- FDA Inspection 1048162 - 2018-03-02

Company: https://www.keypedia.com/companies/mdf-instrumnets-medifriend-inc/c061dfca-c26d-4b2d-9f69-bc16bbc53e15

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