# Micro-Mega SA – FDA Inspection, Dec 7, 2017

Source: https://www.keypedia.com/records/fda_inspections/micro-mega-sa/dad11910-c5ad-417d-97bd-97ad4e739096
Source feed: FDA_Inspections

> FDA inspection 1034461 of Micro-Mega SA, December 07, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1034461
- Company Name: Micro-Mega SA
- Inspection Date: 2017-12-07
- 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: 3

## Related Officers

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

Company: https://www.keypedia.com/companies/micro-mega-sa/f7cf95cc-2fb5-4eb3-9cd3-19ea7739a5e6

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