FDA inspection

Lectro Tek Services Inc: FDA inspection ending Dec 10, 1999

FDA inspection 226 · No Action Indicated (NAI) · Wenatchee, WA

Key facts

Inspection ID 226
Firm Lectro Tek Services Inc
FEI number 3023123
Address 2161
City Wenatchee
State WA
ZIP 98807-2161
Fiscal year 2000
Inspection end date Dec 10, 1999
Classification No Action Indicated (NAI)
Project area Rad Cntrl & Hlth Safety Act (RCHSA) Auth
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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