# FDA Inspection 1223196 - Orthodent Laboratory, Inc. - November 13, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/orthodent-laboratory-inc/0bd84701-1ee9-43ef-8223-f0e668d9998d
Source feed: FDA_Inspections

> FDA Inspection 1223196 for Orthodent Laboratory, Inc. on November 13, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1223196
- Company Name: Orthodent Laboratory, Inc.
- Inspection Date: 2023-11-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1223196 - 2023-11-13](https://www.globalkeysolutions.net/records/fda_inspections/orthodent-laboratory-inc/89255fb1-7f40-4f81-bcc9-e523a705f75f)
- [FDA Inspection 1137122 - 2021-03-24](https://www.globalkeysolutions.net/records/fda_inspections/orthodent-laboratory-inc/e992289f-a30e-4d3a-b354-8f162a791d41)
- [FDA Inspection 1137122 - 2021-03-24](https://www.globalkeysolutions.net/records/fda_inspections/orthodent-laboratory-inc/f9f50106-2197-4b4b-a609-329d5de1f5de)

Company: https://www.globalkeysolutions.net/companies/orthodent-laboratory-inc/9b8304f9-d206-4b2d-89a4-a029f14e1c72

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