FDA inspection

CICOR OHIO, SOLON: FDA inspection ending Oct 29, 2019

FDA inspection 1107979 · Voluntary Action Indicated (VAI) · Solon, OH

Key facts

Inspection ID 1107979
Firm CICOR OHIO, SOLON
FEI number 3010129044
Address 29200 Fountain Pkwy
City Solon
State OH
ZIP 44139
Country United States
Fiscal year 2020
Inspection end date Oct 29, 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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