# Spinalight, Inc. – FDA Inspection, Mar 19, 2015

Source: https://www.keypedia.com/records/fda_inspections/spinalight-inc/95daece1-69f4-49c8-ae67-d0fb0fa11c80
Source feed: FDA_Inspections

> FDA inspection 919385 of Spinalight, Inc., March 19, 2015. Classification: Voluntary Action Indicated (VAI). 9 citations under 21 CFR parts 806 and 820. 3 other FDA inspections on record for this company.

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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)
- 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: 9

## Related Documents

- FDA Inspection 1228191 - 2024-01-31
- [FDA Inspection 792598 - 2012-07-19](https://www.keypedia.com/records/fda_inspections/spinalight-inc/9ffb2255-3eae-4fb3-962d-3281958e4735)
- [FDA Inspection 740084 - 2011-08-18](https://www.keypedia.com/records/fda_inspections/spinalight-inc/7ca36182-c5bd-46f0-8d27-b403849078aa)

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