# Maxilon Laboratories Inc. – FDA Inspection, Mar 7, 2017

Source: https://www.keypedia.com/records/fda_inspections/maxilon-laboratories-inc/a7ab3a1e-a9ae-4a75-ab06-8a88c26f922c
Source feed: FDA_Inspections

> FDA inspection 1003368 of Maxilon Laboratories Inc., March 07, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1003368
- Company Name: Maxilon Laboratories Inc.
- Inspection Date: 2017-03-07
- 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: 1

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/maxilon-laboratories-inc/629a135e-8503-495e-9c40-0404f9ebfd0c

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