FDA inspection

Primus Corporation: FDA inspection ending Feb 6, 2020

FDA inspection 1117396 · Official Action Indicated (OAI) · Kansas City, MO

Key facts

Inspection ID 1117396
Firm Primus Corporation
FEI number 1931251
Address 4231 E 75th Ter
City Kansas City
State MO
ZIP 64132
Country United States
Fiscal year 2020
Inspection end date Feb 6, 2020
Classification Official Action Indicated (OAI)
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
  • 10–99 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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