# FDA Inspection 1029048 - Helena Laboratories, Inc - July 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/helena-laboratories-inc/3fc685ce-e8c5-497e-bce9-11b15b9c86d8
Source feed: FDA_Inspections

> FDA Inspection 1029048 for Helena Laboratories, Inc on July 14, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1029048
- Company Name: Helena Laboratories, Inc
- Inspection Date: 2017-07-14
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## 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 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](https://www.keypedia.com/records/fda_inspections/helena-laboratories-inc/6b0be0ef-91dc-40e4-a8bd-ddab840b0276)
- [FDA Inspection 695366 - 2010-10-28](https://www.keypedia.com/records/fda_inspections/helena-laboratories-inc/e15b5b50-f7f2-49e4-bb65-66a6f378d803)

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