# Anzacare Ltd – FDA Inspection, May 18, 2017

Source: https://www.keypedia.com/records/fda_inspections/anzacare-ltd/f34181cf-94fb-47fb-a791-627463cf5b1d
Source feed: FDA_Inspections

> FDA inspection 1013947 of Anzacare Ltd, May 18, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1013947
- Company Name: Anzacare Ltd
- Inspection Date: 2017-05-18
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/cynthia-t-cain/8b1dcf2b-198c-4218-8cd5-458f62718c1f)

Company: https://www.keypedia.com/companies/anzacare-ltd/cb31667d-3f8e-4bad-bf21-65bdfcdbdf57

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7