# FDA Inspection 1197968 - Luminelle Inc - February 21, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/luminelle-inc/3ffce6f1-5d9a-4cd0-b20b-42d7b7b90b1c
Source feed: FDA_Inspections

> FDA Inspection 1197968 for Luminelle Inc on February 21, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1197968
- Company Name: Luminelle Inc
- Inspection Date: 2023-02-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1197968 - 2023-02-21](https://www.globalkeysolutions.net/records/fda_inspections/luminelle-inc/e33d448f-6627-45a3-a72d-6185f7851744)

Company: https://www.globalkeysolutions.net/companies/luminelle-inc/69e06698-f12d-4400-91de-5a7eb8ea8f60

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