# FDA Inspection 1260617 - Ortec - January 09, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/ortec/fbd92500-709f-409c-a1e1-a0effe612d26/
Source feed: FDA_Inspections

> FDA Inspection 1260617 for Ortec on January 09, 2025. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1260617
- Company Name: Ortec
- Inspection Date: 2025-01-09
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1260617 - 2025-01-09](https://www.globalkeysolutions.net/api/records/fda_inspections/ortec/4159230c-b68b-46f6-b591-375d39ada903/)
- [FDA Inspection 978928 - 2016-01-29](https://www.globalkeysolutions.net/api/records/fda_inspections/ortec/a85c7586-a8f7-4bd6-995f-69681ac0f21e/)
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- [FDA Inspection 663789 - 2010-03-29](https://www.globalkeysolutions.net/api/records/fda_inspections/ortec/9a3e8e0b-6b49-4a89-a5b6-130699fec5af/)

Company: https://www.globalkeysolutions.net/companies/ortec/e7a88df3-0ce8-4995-83ef-628dbc45bd8f

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