# FDA Inspection 919385 - Spinalight, Inc. - March 19, 2015

Source: https://www.keypedia.com/records/fda_inspections/spinalight-inc/032bda62-f2dc-4fc9-8f9e-73a63e05f6b8
Source feed: FDA_Inspections

> FDA Inspection 919385 for Spinalight, Inc. on March 19, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 919385
- Company Name: Spinalight, Inc.
- Inspection Date: 2015-03-19
- 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/spinalight-inc/a41339f9-3026-4de3-822f-20d0e6a4fba2

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