FDA inspection

Carematix, Inc.: FDA inspection ending Dec 19, 2019

FDA inspection 1114844 · No Action Indicated (NAI) · Chicago, IL

Key facts

Inspection ID 1114844
Firm Carematix, Inc.
FEI number 3003982635
Address 209 W Jackson Blvd Ste 401
City Chicago
State IL
ZIP 60602
Country United States
Fiscal year 2020
Inspection end date Dec 19, 2019
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

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