# FDA Inspection 991427 - Percuvision Llc - November 16, 2016

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

> FDA Inspection 991427 for Percuvision Llc on November 16, 2016. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 991427 - 2016-11-16](https://www.globalkeysolutions.net/records/fda_inspections/percuvision-llc/7b709c08-6c77-428c-8667-80491126e12c)
- [FDA Inspection 671901 - 2010-07-14](https://www.globalkeysolutions.net/records/fda_inspections/percuvision-llc/a0232205-d260-40e1-b313-fc5c1b493164)

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

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