FDA inspection

Trident SRL: FDA inspection ending Jun 8, 2023

FDA inspection 1209531 · No Action Indicated (NAI) · Castenedolo

Key facts

Inspection ID 1209531
Firm Trident SRL
FEI number 3012649815
Address Via Artigiani 4
City Castenedolo
Country Italy
Fiscal year 2023
Inspection end date Jun 8, 2023
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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