# FDA Inspection 580472 - Lightmed USA Inc - January 28, 2009

Source: https://www.keypedia.com/records/fda_inspections/lightmed-usa-inc/905538d2-aedb-4d24-853f-4919e0fb647f
Source feed: FDA_Inspections

> FDA Inspection 580472 for Lightmed USA Inc on January 28, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 580472
- Company Name: Lightmed USA Inc
- Inspection Date: 2009-01-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/lightmed-usa-inc/70d7945a-1856-4eed-97d2-3644215b1d7b

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