FDA inspection

Tytex, Inc.: FDA inspection ending May 24, 2006

FDA inspection 433263 · No Action Indicated (NAI) · Lincoln, RI

Key facts

Inspection ID 433263
Firm Tytex, Inc.
FEI number 3000206450
Address 614 George Washington Hwy Ste A2
City Lincoln
State RI
ZIP 02865-4291
Fiscal year 2006
Inspection end date May 24, 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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