# FDA Inspection 820597 - Helena Laboratories, Corp. - March 01, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/helena-laboratories-corp/2b39e363-3d73-4031-b3f5-46b06f89af2e
Source feed: FDA_Inspections

> FDA Inspection 820597 for Helena Laboratories, Corp. on March 01, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 820597
- Company Name: Helena Laboratories, Corp.
- Inspection Date: 2013-03-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 820597 - 2013-03-01](https://www.globalkeysolutions.net/records/fda_inspections/helena-laboratories-corp/92e8404f-4bfd-4aba-8b2d-bf38577293de)

Company: https://www.globalkeysolutions.net/companies/helena-laboratories-corp/9742bc61-dee7-4b93-a33a-0581bd422d44

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