FEI establishment

Cytek Development

FDA establishment FEI 1000292377 · Fremont, United States

Key facts

FEI number 1000292377
Legal name Cytek Development
City Fremont
Country United States
Product types Devices
Last inspection Feb 15, 2006

At a glance

  • 1–9 FDA inspections
  • None No Action Indicated (NAI)
  • 1–9 Voluntary Action Indicated (VAI)
  • None Official Action Indicated (OAI)
  • 1–9 Inspections with a Form 483
  • 10–99 Citations
  • None Repeat citations
  • None Warning letters
  • None Linked 510(k)s

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA establishments (FEI)

An FEI (FDA Establishment Identifier) is the number the FDA assigns to a site it inspects. FEIs of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection and compliance data

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