# FDA Inspection 1082641 - Apelem - January 25, 2019

Source: https://www.keypedia.com/records/fda_inspections/apelem/4ce47e8a-333f-4d77-8f89-83ffe694f8a8
Source feed: FDA_Inspections

> FDA Inspection 1082641 for Apelem on January 25, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1082641
- Company Name: Apelem
- Inspection Date: 2019-01-25
- 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 1082641 - 2019-01-25](https://www.keypedia.com/records/fda_inspections/apelem/6b3244b8-3425-4097-a690-1322a2a46a1b)
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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