FDA inspection

Carehealth America: FDA inspection ending May 19, 2008

FDA inspection 522959 · No Action Indicated (NAI) · Blue Earth, MN

Key facts

Inspection ID 522959
Firm Carehealth America
FEI number 3014946040
Address 1550 Industrial Dr
City Blue Earth
State MN
ZIP 56013-1100
Fiscal year 2008
Inspection end date May 19, 2008
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None Citations
  • None 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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