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FDA inspection

Anderson Caledonia Ltd.: FDA inspection ending May 5, 2017

FDA inspection 1018335 · Voluntary Action Indicated (VAI) · Bellshill

Key facts

Inspection ID 1018335
Firm Anderson Caledonia Ltd.
FEI number 3004530184
Address Caledonian House, Phoenix Crescent
City Bellshill
Fiscal year 2017
Inspection end date May 5, 2017
Classification Voluntary Action Indicated (VAI)
Project area New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|New Drug Evaluation|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices
Product type Devices, Drugs

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.

Other inspections at this establishment

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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