# FDA Inspection 1071279 - Fibralign Corporation - November 08, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/fibralign-corporation/75e27e53-acd6-4d6a-aebb-54fa60b1dcaa
Source feed: FDA_Inspections

> FDA Inspection 1071279 for Fibralign Corporation on November 08, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1071279
- Company Name: Fibralign Corporation
- Inspection Date: 2018-11-08
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1071279 - 2018-11-08](https://www.globalkeysolutions.net/records/fda_inspections/fibralign-corporation/68a5897d-1f1a-4159-91e2-99db0e813987)

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

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