FDA inspection

Biorep Technologies, Inc.: FDA inspection ending Apr 26, 2024

FDA inspection 1239221 · No Action Indicated (NAI) · Miami Lakes, FL

Key facts

Inspection ID 1239221
Firm Biorep Technologies, Inc.
FEI number 3005593675
Address 15804 Nw 57th Ave
City Miami Lakes
State FL
ZIP 33014
Country United States
Fiscal year 2024
Inspection end date Apr 26, 2024
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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

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