# FDA Inspection 1096784 - Anacom General Corporation DBA Anacom MedTek - July 12, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/anacom-general-corporation-dba-anacom-medtek/f87c6f2f-ec6c-4aa6-8aa8-fbb7a8de54f0/
Source feed: FDA_Inspections

> FDA Inspection 1096784 for Anacom General Corporation DBA Anacom MedTek on July 12, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1096784
- Company Name: Anacom General Corporation DBA Anacom MedTek
- Inspection Date: 2019-07-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1096784 - 2019-07-12](https://www.globalkeysolutions.net/api/records/fda_inspections/anacom-general-corporation-dba-anacom-medtek/7da1e1d6-83a1-466d-84a1-849bcef50009/)

Company: https://www.globalkeysolutions.net/companies/anacom-general-corporation-dba-anacom-medtek/8c9ac803-7101-473d-bb5f-d1c903f7b038

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