FDA inspection

Teleflex Medical, Inc.: FDA inspection ending Dec 1, 1999

FDA inspection 10651 · No Action Indicated (NAI) · Jaffrey, NH

Key facts

Inspection ID 10651
Firm Teleflex Medical, Inc.
FEI number 1221019
Address 50 Plantation Dr
City Jaffrey
State NH
ZIP 03452-6631
Fiscal year 2000
Inspection end date Dec 1, 1999
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None Citations
  • None 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

Browse all FDA inspections