# FDA Inspection 1274000 - Fibralign Corporation - June 03, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/fibralign-corporation/8c613646-b968-4585-b69d-dfe7d52ffa4b
Source feed: FDA_Inspections

> FDA Inspection 1274000 for Fibralign Corporation on June 03, 2025. Classification: N/A.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1274000
- Company Name: Fibralign Corporation
- Inspection Date: 2025-06-03
- Product Type: Medical Devices & Rad Health
- Office Name: San Francisco District Office

## Related Documents

- [FDA Inspection 1071279 - 2018-11-08](https://www.globalkeysolutions.net/records/fda_inspections/fibralign-corporation/68a5897d-1f1a-4159-91e2-99db0e813987)
- [FDA Inspection 1071279 - 2018-11-08](https://www.globalkeysolutions.net/records/fda_inspections/fibralign-corporation/75e27e53-acd6-4d6a-aebb-54fa60b1dcaa)

Company: https://www.globalkeysolutions.net/companies/fibralign-corporation/aea695ec-64e0-43f0-89c0-d0ab85079b81

Office: https://www.globalkeysolutions.net/offices/san-francisco-district-office/6f838e9c-aae1-4665-9c46-a51d43be02df