FDA inspection

Needle Specialty Products Corporation: FDA inspection ending Jan 31, 2006

FDA inspection 414656 · No Action Indicated (NAI) · Boyle, MS

Key facts

Inspection ID 414656
Firm Needle Specialty Products Corporation
FEI number 1000112137
Address 600 Highway 446
City Boyle
State MS
ZIP 38730-9673
Fiscal year 2006
Inspection end date Jan 31, 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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