# FDA Inspection 1037789 - PediaLift LLC - January 12, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/pedialift-llc/c7029d13-e1da-476b-9901-539341192cc4
Source feed: FDA_Inspections

> FDA Inspection 1037789 for PediaLift LLC on January 12, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1037789
- Company Name: PediaLift LLC
- Inspection Date: 2018-01-12
- 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 1037789 - 2018-01-12](https://www.globalkeysolutions.net/records/fda_inspections/pedialift-llc/c14c585c-c6e7-41de-bcb2-c1c7ac562af0)

Company: https://www.globalkeysolutions.net/companies/pedialift-llc/13c795f0-3646-4b10-b2f4-67bfa1c93aaf

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