# FDA Inspection 949799 - Helica Instruments, Ltd. - November 11, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/helica-instruments-ltd/fcb0defa-e6e7-4393-8713-817ce5745dc5/
Source feed: FDA_Inspections

> FDA Inspection 949799 for Helica Instruments, Ltd. on November 11, 2015. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 949799
- Company Name: Helica Instruments, Ltd.
- Inspection Date: 2015-11-11
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 949799 - 2015-11-11](https://www.globalkeysolutions.net/api/records/fda_inspections/helica-instruments-ltd/25fd47cc-28d9-4756-8d51-e04296229f1e/)

Company: https://www.globalkeysolutions.net/companies/helica-instruments-ltd/2885d9fb-14de-43c8-b757-c678e0a6b04f

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