FDA inspection

RIO BIOFARMA BRASIL LTDA: FDA inspection ending May 9, 2024

FDA inspection 1238089 · Official Action Indicated (OAI) · Hortolandia

Key facts

Inspection ID 1238089
Firm RIO BIOFARMA BRASIL LTDA
FEI number 3021095601
Address Rodovia Jornalista Francisco Aguirre Proenca, 53
City Hortolandia
Country Brazil
Fiscal year 2024
Inspection end date May 9, 2024
Classification Official Action Indicated (OAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 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

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