FDA inspection

Fibralign Corporation: FDA inspection ending Jun 3, 2025

FDA inspection 1274000 · No Action Indicated (NAI) · Union City, CA

Key facts

Inspection ID 1274000
Firm Fibralign Corporation
FEI number 3013037653
Address 32930 Alvarado Niles Rd Ste 350
City Union City
State CA
ZIP 94587-8109
Fiscal year 2025
Inspection end date Jun 3, 2025
Classification No Action Indicated (NAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

Browse all FDA inspections