FDA inspection

INNOFIBER: FDA inspection ending Mar 26, 2010

FDA inspection 658240 · No Action Indicated (NAI) · Sterling, MA

Key facts

Inspection ID 658240
Firm INNOFIBER
FEI number 3003683459
Address 2 Spratt Technology Dr
City Sterling
State MA
ZIP 01564
Country United States
Fiscal year 2010
Inspection end date Mar 26, 2010
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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