# FDA Inspection 1169619 - Modulight, Inc. - April 22, 2022

Source: https://www.keypedia.com/records/fda_inspections/modulight-inc/8a6e6684-3a1d-44f7-b4ed-821679415d97
Source feed: FDA_Inspections

> FDA Inspection 1169619 for Modulight, Inc. on April 22, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1169619
- Company Name: Modulight, Inc.
- Inspection Date: 2022-04-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1169619 - 2022-04-22](https://www.keypedia.com/records/fda_inspections/modulight-inc/8773e526-5bcc-48b2-9582-cab8aa083f17)

Company: https://www.keypedia.com/companies/modulight-inc/0a174261-2fe7-4bb7-9b1a-481466d8cac3

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