# Percuvision Llc – FDA Inspection, Nov 16, 2016

Source: https://www.keypedia.com/records/fda_inspections/percuvision-llc/99437c62-9e16-445f-86fa-15327263c255
Source feed: FDA_Inspections

> FDA inspection 991427 of Percuvision Llc, November 16, 2016. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 991427
- Company Name: Percuvision Llc
- Inspection Date: 2016-11-16
- 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: 5

## Related Documents

- FDA Inspection 671901 - 2010-07-14

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/rosanna-m-goodrich/44c5c743-f67b-41fe-9cd1-8b5913bf580e)

Company: https://www.keypedia.com/companies/percuvision-llc/07732465-3414-4c90-b13a-587840b4ef31

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