# FDA Inspection 1031751 - LPG Systems - May 18, 2017

Source: https://www.keypedia.com/records/fda_inspections/lpg-systems/2ffdf06a-9298-47cc-b596-b16eeb5cf9f1
Source feed: FDA_Inspections

> FDA Inspection 1031751 for LPG Systems on May 18, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031751
- Company Name: LPG Systems
- Inspection Date: 2017-05-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 841228 - 2013-06-27](https://www.keypedia.com/records/fda_inspections/lpg-systems/556f50ed-7664-486d-a12e-81f7aaadef9e)
- [FDA Inspection 841228 - 2013-06-27](https://www.keypedia.com/records/fda_inspections/lpg-systems/627b4d62-2db9-4095-b0fd-4c4a9d0778eb)

Company: https://www.keypedia.com/companies/lpg-systems/db10e87e-1dc1-4ddc-9774-d3e325480b50

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