# FDA Inspection 1089163 - MobileHelp, LLC - May 07, 2019

Source: https://www.keypedia.com/records/fda_inspections/mobilehelp-llc/5330fc17-bd9e-4009-a513-b8a2631a0b60
Source feed: FDA_Inspections

> FDA Inspection 1089163 for MobileHelp, LLC on May 07, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1089163
- Company Name: MobileHelp, LLC
- Inspection Date: 2019-05-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1164271 - 2022-03-11](https://www.keypedia.com/records/fda_inspections/mobilehelp-llc/156cacbc-2b35-46d2-979e-1fbed5947f16)
- [FDA Inspection 1164271 - 2022-03-11](https://www.keypedia.com/records/fda_inspections/mobilehelp-llc/38a11c09-5e0a-40ec-b9b2-41fedf1d48b2)
- [FDA Inspection 1089163 - 2019-05-07](https://www.keypedia.com/records/fda_inspections/mobilehelp-llc/27729669-cef2-4633-9306-92a0824db1bc)

Company: https://www.keypedia.com/companies/mobilehelp-llc/e399dbe5-2838-440c-8ef9-7fcc0473a643

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