# Helena Laboratories, Inc – FDA Inspection, Jul 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/helena-laboratories-inc/a34123e3-12c8-49d5-af1c-14993ba858c7
Source feed: FDA_Inspections

> FDA inspection 1029048 of Helena Laboratories, Inc, July 14, 2017. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029048
- Company Name: Helena Laboratories, Inc
- Inspection Date: 2017-07-14
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 820619 - 2013-03-01](https://www.keypedia.com/records/fda_inspections/helena-laboratories-inc/a49a205c-307b-4096-9d43-4161856e8725)
- FDA Inspection 695366 - 2010-10-28

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/ellen-j-tave/a70cd3ed-957f-471b-82ff-24ca7c65bc10)

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