FDA inspection

Tulsa Dental Products LLC: FDA inspection ending Jul 29, 2016

FDA inspection 980654 · Voluntary Action Indicated (VAI) · Johnson City, TN

Key facts

Inspection ID 980654
Firm Tulsa Dental Products LLC
FEI number 1000554802
Address 608 Rolling Hills Dr
City Johnson City
State TN
ZIP 37604
Country United States
Fiscal year 2016
Inspection end date Jul 29, 2016
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 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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