FDA inspection

Tulsa Dental Products LLC dba Tulsa Dental Specialties: FDA inspection ending May 20, 2004

FDA inspection 329890 · No Action Indicated (NAI) · Tulsa, OK

Key facts

Inspection ID 329890
Firm Tulsa Dental Products LLC dba Tulsa Dental Specialties
FEI number 1643003
Address 5100 E Skelly Dr Ste 300
City Tulsa
State OK
ZIP 74135-6560
Fiscal year 2004
Inspection end date May 20, 2004
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