FDA inspection

KEOS LLC: FDA inspection ending Aug 23, 2019

FDA inspection 1100408 · Voluntary Action Indicated (VAI) · Lancaster, PA

Key facts

Inspection ID 1100408
Firm KEOS LLC
FEI number 3013921069
Address 1824 Colonial Village Ln
City Lancaster
State PA
ZIP 17601
Country United States
Fiscal year 2019
Inspection end date Aug 23, 2019
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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