FDA inspection

Cellay, Inc: FDA inspection ending Jun 18, 2010

FDA inspection 667333 · No Action Indicated (NAI) · Cambridge, MA

Key facts

Inspection ID 667333
Firm Cellay, Inc
FEI number 3007738260
Address 100 Inman St Ste 200
City Cambridge
State MA
ZIP 02139
Country United States
Fiscal year 2010
Inspection end date Jun 18, 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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