# Apelem – FDA Inspection, Jan 25, 2019

Source: https://www.keypedia.com/records/fda_inspections/apelem/6b3244b8-3425-4097-a690-1322a2a46a1b
Source feed: FDA_Inspections

> FDA inspection 1082641 of Apelem, January 25, 2019. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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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)
- Classification Code: NAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1194056 - 2022-12-08
- [FDA Inspection 1002222 - 2017-01-26](https://www.keypedia.com/records/fda_inspections/apelem/60171ec2-1ae8-4dd8-8d15-c48029bdb86d)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/jennifer-s-ness/532f8a81-e393-4e83-b5f2-a72362e966de)

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