# RDI Inc. – FDA Inspection, Jun 10, 2019

Source: https://www.keypedia.com/records/fda_inspections/rdi-inc/890ca456-abec-473d-b30e-2a6bb49ff246
Source feed: FDA_Inspections

> FDA inspection 1092436 of RDI Inc., June 10, 2019. 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: 1092436
- Company Name: RDI Inc.
- Inspection Date: 2019-06-10
- 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 1261930 - 2025-02-13

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/andrew-j-garufi/567f6aaa-f6f2-45a3-9a58-80b33f3ad021)

Company: https://www.keypedia.com/companies/rdi-inc/56067983-86bf-46a9-9c9e-6824dd7f13a9

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