# FDA Inspection 986804 - ProNuVis LLC - September 19, 2016

Source: https://www.keypedia.com/records/fda_inspections/pronuvis-llc/8354bde6-db69-4d69-a15e-016deca680e7
Source feed: FDA_Inspections

> FDA Inspection 986804 for ProNuVis LLC on September 19, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 986804
- Company Name: ProNuVis LLC
- Inspection Date: 2016-09-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/pronuvis-llc/dabb6a5f-44f1-4fc6-abd6-8a727299de5b

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