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

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

> FDA Inspection 1059203 for Helena Laboratories UK Ltd on July 18, 2018. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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