# FDA Inspection 1079030 - Memtec Incorporated - February 04, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/memtec-incorporated/dea4872d-20e5-4341-b575-cfabfb0f7d3e
Source feed: FDA_Inspections

> FDA Inspection 1079030 for Memtec Incorporated on February 04, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1079030
- Company Name: Memtec Incorporated
- Inspection Date: 2019-02-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1151504 - 2021-08-06](https://www.globalkeysolutions.net/records/fda_inspections/memtec-incorporated/1268006b-9fb1-455c-a163-4112e29ed55f)
- [FDA Inspection 1151504 - 2021-08-06](https://www.globalkeysolutions.net/records/fda_inspections/memtec-incorporated/696631b1-083e-464b-81f4-b32cd3417f36)
- [FDA Inspection 1079030 - 2019-02-04](https://www.globalkeysolutions.net/records/fda_inspections/memtec-incorporated/4cd921f7-c523-4371-933b-e827da7441fc)
- [FDA Inspection 949589 - 2015-11-20](https://www.globalkeysolutions.net/records/fda_inspections/memtec-incorporated/bef2ea35-339c-4821-b176-fb9584fa3ce5)
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Company: https://www.globalkeysolutions.net/companies/memtec-incorporated/fe124472-b57f-4ff9-ae9d-2327222b5fc8

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