# FDA Inspection 1100866 - LightVision Technologies Corp - June 03, 2019

Source: https://www.keypedia.com/records/fda_inspections/lightvision-technologies-corp/b5079756-47cc-4937-b6aa-d840a0b8504b
Source feed: FDA_Inspections

> FDA Inspection 1100866 for LightVision Technologies Corp on June 03, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1100866
- Company Name: LightVision Technologies Corp
- Inspection Date: 2019-06-03
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 984969 - 2016-06-21](https://www.keypedia.com/records/fda_inspections/lightvision-technologies-corp/5c7c02aa-675e-4bdf-a3f7-f5a4bfe9ec36)
- [FDA Inspection 719932 - 2010-11-15](https://www.keypedia.com/records/fda_inspections/lightvision-technologies-corp/70071846-5163-4511-b945-f754a0848022)
- [FDA Inspection 583444 - 2009-04-09](https://www.keypedia.com/records/fda_inspections/lightvision-technologies-corp/08ffc7d0-6cb6-4db7-88b7-fd38e06457fa)

Company: https://www.keypedia.com/companies/lightvision-technologies-corp/fe58cb87-d69b-4305-b624-54979676d814

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