# FDA Inspection 846387 - Lightwave - August 08, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/lightwave/301c48f4-4364-4190-b0e6-bf7ae7bedb36
Source feed: FDA_Inspections

> FDA Inspection 846387 for Lightwave on August 08, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 846387
- Company Name: Lightwave
- Inspection Date: 2013-08-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/lightwave/ab86405c-ae8f-4ab3-b9ae-dc51352e9a61

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