# Anacom General Corporation – FDA Inspection, Jul 12, 2019

Source: https://www.keypedia.com/records/fda_inspections/anacom-general-corporation/f87c6f2f-ec6c-4aa6-8aa8-fbb7a8de54f0
Source feed: FDA_Inspections

> FDA inspection 1096784 of Anacom General Corporation, July 12, 2019. Classification: Voluntary Action Indicated (VAI). 9 citations under 21 CFR parts 803 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1096784
- Company Name: Anacom General Corporation
- Inspection Date: 2019-07-12
- 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: 9

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/matthew-d-schnittker/cf76f07f-db6d-47a0-8412-7eb084d4fe8b)

Company: https://www.keypedia.com/companies/anacom-general-corporation/8c9ac803-7101-473d-bb5f-d1c903f7b038

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