# Bioretec Ltd – FDA Inspection, Feb 22, 2018

Source: https://www.keypedia.com/records/fda_inspections/bioretec-ltd/4ff17489-5157-427b-98ef-bcd149210430
Source feed: FDA_Inspections

> FDA inspection 1044937 of Bioretec Ltd, February 22, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation 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: 1044937
- Company Name: Bioretec Ltd
- Inspection Date: 2018-02-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1259316 - 2025-01-23](https://www.keypedia.com/records/fda_inspections/bioretec-ltd/9bbdbcc3-db5d-455b-bd15-19291a42cd23)

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/bioretec-ltd/34ca33da-554b-4198-852d-1b35a87fdf1e

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