FDA inspection

ZiphyCare, Inc.: FDA inspection ending Nov 2, 2015

FDA inspection 948362 · Voluntary Action Indicated (VAI) · New York, NY

Key facts

Inspection ID 948362
Firm ZiphyCare, Inc.
FEI number 3011682748
Address 315 W 36th St
City New York
State NY
ZIP 10001
Country United States
Fiscal year 2016
Inspection end date Nov 2, 2015
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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