FDA inspection

Zipline Medical: FDA inspection ending Feb 28, 2020

FDA inspection 1121679 · No Action Indicated (NAI) · Campbell, CA

Key facts

Inspection ID 1121679
Firm Zipline Medical
FEI number 3009673389
Address 747 Camden Ave Ste A
City Campbell
State CA
ZIP 95008
Country United States
Fiscal year 2020
Inspection end date Feb 28, 2020
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

Browse all FDA inspections