# Respitek (Pty) Ltd – FDA Inspection, Feb 11, 2016

Source: https://www.keypedia.com/records/fda_inspections/respitek-pty-ltd/687819ea-e38a-4fc0-bdae-c481f97e43fd
Source feed: FDA_Inspections

> FDA inspection 958327 of Respitek (Pty) Ltd, February 11, 2016. Classification: Voluntary Action Indicated (VAI). 11 citations under 21 CFR parts 803 and 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 958327
- Company Name: Respitek (Pty) Ltd
- Inspection Date: 2016-02-11
- 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: 11

Company: https://www.keypedia.com/companies/respitek-pty-ltd/ee8afb92-9469-4dfb-8e6b-65c7df544ff5

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