# FDA Inspection 1271183 - Tendonova Corporation - May 16, 2025

Source: https://www.keypedia.com/records/fda_inspections/tendonova-corporation/3e70a27e-09e3-4e71-be86-95f958cf8194
Source feed: FDA_Inspections

> FDA Inspection 1271183 for Tendonova Corporation on May 16, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1271183
- Company Name: Tendonova Corporation
- Inspection Date: 2025-05-16
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1271183 - 2025-05-16](https://www.keypedia.com/records/fda_inspections/tendonova-corporation/14b66088-e323-40e8-8d0a-3f560d705128)
- [FDA Inspection 1271183 - 2025-05-16](https://www.keypedia.com/records/fda_inspections/tendonova-corporation/c0687c78-4464-482f-bc43-90ceccd8b868)

Company: https://www.keypedia.com/companies/tendonova-corporation/e7d13901-1914-4899-a9d2-140e1235bbdc

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