# Helica Instruments, Ltd. – FDA Inspection, Nov 11, 2015

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

> FDA inspection 949799 of Helica Instruments, Ltd., November 11, 2015. Classification: Official Action Indicated (OAI). 12 citations under 21 CFR parts 803 and 820.

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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)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 12

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

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