# LPG Systems – FDA Inspection, 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 of LPG Systems, May 18, 2017. 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: 1031751
- Company Name: LPG Systems
- Inspection Date: 2017-05-18
- 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 841228 - 2013-06-27

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/adaliz-santaliz-cruz/47bd4220-e6cc-4582-a4f5-bd4337f92622)

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