# Intermedic Arfran S.A. – FDA Inspection, Feb 5, 2016

Source: https://www.keypedia.com/records/fda_inspections/intermedic-arfran-sa/d6f4093a-2562-41f9-b3db-4ab6ade2480d
Source feed: FDA_Inspections

> FDA inspection 958881 of Intermedic Arfran S.A., February 05, 2016. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 820, 1002 and 1010. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 958881
- Company Name: Intermedic Arfran S.A.
- Inspection Date: 2016-02-05
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- FDA Inspection 1110941 - 2019-11-14

Company: https://www.keypedia.com/companies/intermedic-arfran-sa/ff91ad41-f31f-4e03-b74b-beb6ca629004

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