Compliance document

Form FDA 483: NextPhase Medical Devices

FDA FOIA

Key facts

Document type Form FDA 483
Firm NextPhase Medical Devices
FEI number 3002882053
Inspection 787295
Collection FDA FOIA

At a glance

  • 1–9 Pages
  • 1–9 FDA inspections at this FEI

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

About FDA inspection and compliance documents

The Orca1 document library indexes FDA compliance documents such as Form 483 observations, establishment inspection reports and firm responses. Documents are available to Orca1 subscribers only.

Source: U.S. Food and Drug Administration (FDA) records, Orca1 document library

Browse all FDA inspection and compliance documents