# FDA Inspection 1304188 - Ortho2 - February 04, 2026

Source: https://www.globalkeysolutions.net/records/fda_inspections/ortho2/f6dabfd7-a019-4fa1-a8b8-5195ed01f8b3/
Source feed: FDA_Inspections

> FDA Inspection 1304188 for Ortho2 on February 04, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1304188
- Company Name: Ortho2
- Inspection Date: 2026-02-04
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices

## Related Documents

- [FDA Inspection 1304188 - 2026-02-04](https://www.globalkeysolutions.net/api/records/fda_inspections/ortho2/5cb3ae65-4996-4cd2-9ed1-138868caf89a/)
- [FDA Inspection 1304188 - 2026-02-04](https://www.globalkeysolutions.net/api/records/fda_inspections/ortho2/d38e0306-44ad-4977-9027-756edf8f5e2f/)
- [FDA Inspection 1192361 - 2022-12-01](https://www.globalkeysolutions.net/api/records/fda_inspections/ortho2/c0c7e045-dbe9-47f9-aef8-66f6d2e3ab51/)
- [FDA Inspection 1192361 - 2022-12-01](https://www.globalkeysolutions.net/api/records/fda_inspections/ortho2/b92c600c-d501-4d2e-ab35-fd3bf7f1308e/)

Company: https://www.globalkeysolutions.net/companies/ortho2/9b9a70f2-4422-4ea0-8411-96cddcf00e90