# FDA Inspection 987962 - FloSpine, LLC - September 29, 2016

Source: https://www.keypedia.com/records/fda_inspections/flospine-llc/41504c60-12a4-4b33-9ec5-e3076d371cc9
Source feed: FDA_Inspections

> FDA Inspection 987962 for FloSpine, LLC on September 29, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 987962
- Company Name: FloSpine, LLC
- Inspection Date: 2016-09-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/flospine-llc/176eb880-b349-4042-86d5-dddeee7a6a01

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