FDA inspection

Eaton Manufacturing Corporation Dba Eaton Medical: FDA inspection ending Aug 17, 2004

FDA inspection 343625 · No Action Indicated (NAI) · Memphis, TN

Key facts

Inspection ID 343625
Firm Eaton Manufacturing Corporation Dba Eaton Medical
FEI number 1000113105
Address 1401 Heistan Pl
City Memphis
State TN
ZIP 38104-4729
Fiscal year 2004
Inspection end date Aug 17, 2004
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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