# SmartGuard Rx, Inc. – FDA Inspection, Dec 12, 2018

Source: https://www.keypedia.com/records/fda_inspections/smartguard-rx-inc/84536e4f-9b6b-415b-bbbc-b5d065266a38
Source feed: FDA_Inspections

> FDA inspection 1074288 of SmartGuard Rx, Inc., December 12, 2018. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR parts 803 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1074288
- Company Name: SmartGuard Rx, Inc.
- Inspection Date: 2018-12-12
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/james-r-montero/ce2d19fd-25b7-423e-9132-5d6f582380d2)

Company: https://www.keypedia.com/companies/smartguard-rx-inc/586e005d-e99c-471e-bc81-c5accb464a26

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