# Lightmed USA Inc – FDA Inspection, Jun 27, 2017

Source: https://www.keypedia.com/records/fda_inspections/lightmed-usa-inc/7ad7d985-6355-4be2-b967-a269699b4c3e
Source feed: FDA_Inspections

> FDA inspection 1016667 of Lightmed USA Inc, June 27, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1016667
- Company Name: Lightmed USA Inc
- Inspection Date: 2017-06-27
- 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: 2

## Related Documents

- FDA Inspection 1217913 - 2023-08-09
- FDA Inspection 580472 - 2009-01-28

## Related Officers

- [Company Rep](https://www.keypedia.com/people/sarah-a-hassas/4f142d54-fc28-4bd5-82ad-7e6fa443688c)

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