FEI establishment

CoreRX Inc.

FDA establishment FEI 3007209985 · Clearwater, United States

Key facts

FEI number 3007209985
Legal name CoreRX Inc.
City Clearwater
Country United States
Product types Biologics, Drugs
Drug operations ANALYSIS, LABEL, MANUFACTURE, PACK
Last inspection Feb 26, 2026

At a glance

  • 10–99 FDA inspections
  • 1–9 No Action Indicated (NAI)
  • 1–9 Voluntary Action Indicated (VAI)
  • 1–9 Official Action Indicated (OAI)
  • 10–99 Inspections with a Form 483
  • 10–99 Citations
  • 10–99 Repeat citations
  • None Warning letters
  • None Linked 510(k)s

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

About FDA establishments (FEI)

An FEI (FDA Establishment Identifier) is the number the FDA assigns to a site it inspects. FEIs of individual clinical investigators are not published here.

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

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