FDA inspection

Oxavita SRL: FDA inspection ending Feb 2, 2024

FDA inspection 1231715 · No Action Indicated (NAI) · Buenos Aires

Key facts

Inspection ID 1231715
Firm Oxavita SRL
FEI number 3016489995
Address Ceretti 3320 Caba
City Buenos Aires
Country Argentina
Fiscal year 2024
Inspection end date Feb 2, 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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