# FDA Inspection 1013125 - Roll Recovery, LLC - June 06, 2017

Source: https://www.keypedia.com/records/fda_inspections/roll-recovery-llc/5e595d40-ed2f-4df8-9cdc-f166aa66689e
Source feed: FDA_Inspections

> FDA Inspection 1013125 for Roll Recovery, LLC on June 06, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1013125
- Company Name: Roll Recovery, LLC
- Inspection Date: 2017-06-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1013125 - 2017-06-06](https://www.keypedia.com/records/fda_inspections/roll-recovery-llc/7c6c9677-fda6-42fd-806f-c07a8895a298)

Company: https://www.keypedia.com/companies/roll-recovery-llc/e1400ac2-5adc-4889-a87a-363a9bab6398

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