# Piezosurgery Inc – FDA Inspection, Mar 1, 2011

Source: https://www.keypedia.com/records/fda_inspections/piezosurgery-inc/4eaa0abd-f7ae-4049-9d20-8cd341871c05
Source feed: FDA_Inspections

> FDA inspection 712899 of Piezosurgery Inc, March 01, 2011. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 712899
- Company Name: Piezosurgery Inc
- Inspection Date: 2011-03-01
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- [FDA Inspection 1017087 - 2017-06-28](https://www.keypedia.com/records/fda_inspections/piezosurgery-inc/ad870d6a-6388-42d4-bce1-de810746e69c)
- FDA Inspection 860088 - 2013-12-16
- [FDA Inspection 759923 - 2011-12-13](https://www.keypedia.com/records/fda_inspections/piezosurgery-inc/a7732dd1-368b-4a69-9dd7-8d75a6d3a9da)
- [FDA Inspection 656861 - 2010-04-12](https://www.keypedia.com/records/fda_inspections/piezosurgery-inc/256c4b93-2344-4db5-b22c-e871dc187ee0)

Company: https://www.keypedia.com/companies/piezosurgery-inc/25c9540e-3b72-4b70-ab53-6a361d45bd6b

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