# FDA Inspection 977039 - Kapitex Healthcare Ltd - February 10, 2016

Source: https://www.keypedia.com/records/fda_inspections/kapitex-healthcare-ltd/ae6c0781-0cbb-4201-8a09-80bb700a76d6
Source feed: FDA_Inspections

> FDA Inspection 977039 for Kapitex Healthcare Ltd on February 10, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 977039
- Company Name: Kapitex Healthcare Ltd
- Inspection Date: 2016-02-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/kapitex-healthcare-ltd/2ecc7dac-1380-40a7-8c38-30342bae6b12

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