# Iotron Technologies Inc – FDA Inspection, May 23, 2013

Source: https://www.keypedia.com/records/fda_inspections/iotron-technologies-inc/917e2cf7-ab04-45f1-8081-04bb3964f86d
Source feed: FDA_Inspections

> FDA inspection 841553 of Iotron Technologies Inc, May 23, 2013. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 841553
- Company Name: Iotron Technologies Inc
- Inspection Date: 2013-05-23
- 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: 4

Company: https://www.keypedia.com/companies/iotron-technologies-inc/65c48992-e237-47de-be74-4d1781f6efc6

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