# Apelem – FDA Inspection, Jan 26, 2017

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

> FDA inspection 1002222 of Apelem, January 26, 2017. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- FDA Inspection 1194056 - 2022-12-08
- [FDA Inspection 1082641 - 2019-01-25](https://www.keypedia.com/records/fda_inspections/apelem/6b3244b8-3425-4097-a690-1322a2a46a1b)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/rosanna-m-goodrich/44c5c743-f67b-41fe-9cd1-8b5913bf580e)

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