# FDA Inspection 1059203 - Helena Laboratories UK Ltd - July 18, 2018

Source: https://www.keypedia.com/records/fda_inspections/helena-laboratories-uk-ltd/245a04ab-0aa4-44ef-8e6c-6e9f6f74e49f
Source feed: FDA_Inspections

> FDA inspection 1059203 of Helena Laboratories UK Ltd, July 18, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1059203
- Company Name: Helena Laboratories UK Ltd
- Inspection Date: 2018-07-18
- 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: 2

## Related Documents

- [FDA Inspection 1258084 - 2025-01-09](https://www.keypedia.com/records/fda_inspections/helena-laboratories-uk-ltd/23e018da-62ec-4778-a729-bc26072b5640)

Company: https://www.keypedia.com/companies/helena-laboratories-uk-ltd/04615ff8-2f17-4e35-abf5-8e0ae068dc55

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