FDA inspection

Bioplate Inc: FDA inspection ending Sep 1, 2011

FDA inspection 743472 · No Action Indicated (NAI) · Placentia, CA

Key facts

Inspection ID 743472
Firm Bioplate Inc
FEI number 1000518793
Address 570 S Melrose St
City Placentia
State CA
ZIP 92870
Country United States
Fiscal year 2011
Inspection end date Sep 1, 2011
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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