FDA inspection

Cellay, Inc: FDA inspection ending Feb 10, 2016

FDA inspection 960939 · Voluntary Action Indicated (VAI) · Cambridge, MA

Key facts

Inspection ID 960939
Firm Cellay, Inc
FEI number 3007738260
Address 100 Inman Street, Ste 200
City Cambridge
State MA
ZIP 02139
Country United States
Fiscal year 2016
Inspection end date Feb 10, 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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