# Fibralign Corporation – FDA Inspection, Nov 8, 2018

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

> FDA inspection 1071279 of Fibralign Corporation, November 08, 2018. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1274000 - 2025-06-03

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/quynh-strandberg/9b582ae6-85f9-4163-8ce6-b179c5fd340e)

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

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