# FDA Inspection 940228 - Arrotek Medical Ltd - July 30, 2015

Source: https://www.keypedia.com/records/fda_inspections/arrotek-medical-ltd/e7b44094-98bb-40b4-9588-73a9e9296d4e
Source feed: FDA_Inspections

> FDA Inspection 940228 for Arrotek Medical Ltd on July 30, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 940228
- Company Name: Arrotek Medical Ltd
- Inspection Date: 2015-07-30
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 940228 - 2015-07-30](https://www.keypedia.com/records/fda_inspections/arrotek-medical-ltd/40af8eae-cb77-4b24-a199-51f22e49c31a)

Company: https://www.keypedia.com/companies/arrotek-medical-ltd/ab859c35-ebc7-42a0-8677-b1b564a2a6d7

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