# FDA Inspection 1002222 - Apelem - January 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/apelem/60171ec2-1ae8-4dd8-8d15-c48029bdb86d
Source feed: FDA_Inspections

> FDA Inspection 1002222 for Apelem on January 26, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1002222
- Company Name: Apelem
- Inspection Date: 2017-01-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/apelem/64c64f08-6d00-4737-9e3b-6261487beb68

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