# FDA Inspection 1054770 - Reavillmed, Llc - April 27, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/reavillmed-llc/4ef7508f-f868-47d7-907e-5e487be8ae32
Source feed: FDA_Inspections

> FDA Inspection 1054770 for Reavillmed, Llc on April 27, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1054770
- Company Name: Reavillmed, Llc
- Inspection Date: 2018-04-27
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1054770 - 2018-04-27](https://www.globalkeysolutions.net/records/fda_inspections/reavillmed-llc/7c7d368b-9f24-45a7-b9e4-359eac71f2f9)
- [FDA Inspection 678197 - 2010-08-19](https://www.globalkeysolutions.net/records/fda_inspections/reavillmed-llc/c1d24faa-bbb1-404d-a7f0-a54007a819c4)

Company: https://www.globalkeysolutions.net/companies/reavillmed-llc/3c954b7a-af1f-40a7-9a1b-f84b105852da

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