# FDA Inspection 802862 - Lightwave - September 21, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/lightwave/0856dd97-97bf-4244-9930-4e099590b29e
Source feed: FDA_Inspections

> FDA Inspection 802862 for Lightwave on September 21, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 802862
- Company Name: Lightwave
- Inspection Date: 2012-09-21
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: 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