FDA inspection

Becton Dickinson Vacutainer Systems: FDA inspection ending Nov 16, 2017

FDA inspection 1052936 · No Action Indicated (NAI) · Plymouth

Key facts

Inspection ID 1052936
Firm Becton Dickinson Vacutainer Systems
FEI number 3002806485
Address Belliver Way, Indust Estate
City Plymouth
Fiscal year 2018
Inspection end date Nov 16, 2017
Classification No Action Indicated (NAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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