# Memtec Incorporated – FDA Inspection, Feb 4, 2019

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

> FDA inspection 1079030 of Memtec Incorporated, February 04, 2019. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. Form 483 issued. 5 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 1151504 - 2021-08-06
- FDA Inspection 949589 - 2015-11-20
- FDA Inspection 854123 - 2013-11-06
- FDA Inspection 752409 - 2011-10-31
- FDA Inspection 572524 - 2009-03-26

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/memtec-incorporated/fe124472-b57f-4ff9-ae9d-2327222b5fc8

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