FDA inspection

Pulpdent Corporation: FDA inspection ending Jun 21, 2000

FDA inspection 29261 · Voluntary Action Indicated (VAI) · Watertown, MA

Key facts

Inspection ID 29261
Firm Pulpdent Corporation
FEI number 1215305
Address 46 Acton St
City Watertown
State MA
ZIP 02472-2208
Fiscal year 2000
Inspection end date Jun 21, 2000
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None 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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