# Nuvolase Inc. – FDA Inspection, May 23, 2018

Source: https://www.keypedia.com/records/fda_inspections/nuvolase-inc/701507da-e88e-494d-8e87-f843dea4599c
Source feed: FDA_Inspections

> FDA inspection 1052985 of Nuvolase Inc., May 23, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 820 and 1002. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1052985
- Company Name: Nuvolase Inc.
- Inspection Date: 2018-05-23
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 917181 - 2015-03-13
- [FDA Inspection 850450 - 2013-09-20](https://www.keypedia.com/records/fda_inspections/nuvolase-inc/e39ed00f-02a6-41a1-8ecd-d8b518030c6e)
- FDA Inspection 652943 - 2010-05-03

## Related Officers

- [Company Rep](https://www.keypedia.com/people/christine-i-shaw/480cb61e-f173-432d-b84a-c8b492192302)

Company: https://www.keypedia.com/companies/nuvolase-inc/ce2cec64-0104-45aa-9ac4-98aefe7e3e1f

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