FDA inspection

LOHMAN TECHNOLOGIES LLC: FDA inspection ending Sep 27, 2024

FDA inspection 1250230 · Voluntary Action Indicated (VAI) · Pewaukee, WI

Key facts

Inspection ID 1250230
Firm LOHMAN TECHNOLOGIES LLC
FEI number 3012267350
Address N27w23953 Paul Rd Ste 204
City Pewaukee
State WI
ZIP 53072
Country United States
Fiscal year 2024
Inspection end date Sep 27, 2024
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 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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