FDA inspection

Lemco Enterprises, Inc: FDA inspection ending Feb 1, 2005

FDA inspection 366610 · No Action Indicated (NAI) · Ardmore, OK

Key facts

Inspection ID 366610
Firm Lemco Enterprises, Inc
FEI number 1000117748
Address 3204 Hale Rd
City Ardmore
State OK
ZIP 73401-3740
Fiscal year 2005
Inspection end date Feb 1, 2005
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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