FDA inspection

Gibson Laboratories, LLC: FDA inspection ending Dec 12, 2013

FDA inspection 859677 · Voluntary Action Indicated (VAI) · Lexington, KY

Key facts

Inspection ID 859677
Firm Gibson Laboratories, LLC
FEI number 1050138
Address 1040 Manchester St
City Lexington
State KY
ZIP 40508
Country United States
Fiscal year 2014
Inspection end date Dec 12, 2013
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None 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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