# Helena Laboratories, Inc – FDA Inspection, Mar 1, 2013

Source: https://www.keypedia.com/records/fda_inspections/helena-laboratories-inc/a49a205c-307b-4096-9d43-4161856e8725
Source feed: FDA_Inspections

> FDA inspection 820619 of Helena Laboratories, Inc, March 01, 2013. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 820619
- Company Name: Helena Laboratories, Inc
- Inspection Date: 2013-03-01
- 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 1029048 - 2017-07-14](https://www.keypedia.com/records/fda_inspections/helena-laboratories-inc/a34123e3-12c8-49d5-af1c-14993ba858c7)
- FDA Inspection 695366 - 2010-10-28

Company: https://www.keypedia.com/companies/helena-laboratories-inc/9fec945b-1553-4aed-9026-6cc02a33a43a

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