# LaunchPOrt Llc – FDA Inspection, Jul 24, 2019

Source: https://www.keypedia.com/records/fda_inspections/launchport-llc/0bfd739d-d663-4344-b9e5-fbe8d9ab7156
Source feed: FDA_Inspections

> FDA inspection 1097310 of LaunchPOrt Llc, July 24, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1097310
- Company Name: LaunchPOrt Llc
- Inspection Date: 2019-07-24
- 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: 2

## Related Documents

- FDA Inspection 1250892 - 2024-09-11

## Related Officers

- [Investigator](https://www.keypedia.com/people/jude-c-dike/ea760122-1121-420a-9875-c49de6f3bb0e)

Company: https://www.keypedia.com/companies/launchport-llc/1ecb7f81-ba2d-49a8-a162-624c8519f0c9

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