# Misonix, Inc. – FDA Inspection, Dec 14, 2015

Source: https://www.keypedia.com/records/fda_inspections/misonix-inc/717bf6d4-54de-4652-b030-24a2ac0ffb03
Source feed: FDA_Inspections

> FDA inspection 952742 of Misonix, Inc., December 14, 2015. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 952742
- Company Name: Misonix, Inc.
- Inspection Date: 2015-12-14
- 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

- FDA Inspection 1017560 - 2017-05-19
- [FDA Inspection 898643 - 2014-10-10](https://www.keypedia.com/records/fda_inspections/misonix-inc/cf83c967-a408-4f62-b85f-412679dbe589)
- FDA Inspection 781232 - 2012-04-26
- FDA Inspection 657067 - 2010-03-25

Company: https://www.keypedia.com/companies/misonix-inc/4833fb5c-8af1-4ff4-b5f4-60b01e0fa540

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