# ANDERSEN CALEDONIA LTD – FDA Inspection, May 5, 2017

Source: https://www.keypedia.com/records/fda_inspections/andersen-caledonia-ltd/2aae7d4c-0bc3-4377-a0db-8a6ae4e48355
Source feed: FDA_Inspections

> FDA inspection 1018335 of ANDERSEN CALEDONIA LTD, May 05, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1018335
- Company Name: ANDERSEN CALEDONIA LTD
- Inspection Date: 2017-05-05
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Human Drugs
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 5

## Related Documents

- [FDA Inspection 1284256 - 2025-09-18](https://www.keypedia.com/records/fda_inspections/andersen-caledonia-ltd/99b17aad-2862-47d5-aa5c-6db79ce749f8)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/camerson-e-moore/50733244-0d55-4b0b-a758-f192b7c66457)

Company: https://www.keypedia.com/companies/andersen-caledonia-ltd/f73ef72c-47f0-4f5d-8223-da95df23dfa4

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8