FDA inspection

Deringer-Ney, Inc.: FDA inspection ending Jan 13, 2006

FDA inspection 411551 · No Action Indicated (NAI) · Bloomfield, CT

Key facts

Inspection ID 411551
Firm Deringer-Ney, Inc.
FEI number 1218814
Address 65 W Dudley Town Rd
City Bloomfield
State CT
ZIP 06002-1376
Fiscal year 2006
Inspection end date Jan 13, 2006
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

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