FDA inspection

Lifeaire Systems: FDA inspection ending Aug 29, 2023

FDA inspection 1216203 · Voluntary Action Indicated (VAI) · Shoemakersville, PA

Key facts

Inspection ID 1216203
Firm Lifeaire Systems
FEI number 3009065312
Address 1275 Glenlivet Dr Ste 100
City Shoemakersville
State PA
ZIP 19555
Country United States
Fiscal year 2023
Inspection end date Aug 29, 2023
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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