# Inter Bio-Lab, Inc. – FDA Inspection, Dec 5, 2019

Source: https://www.keypedia.com/records/fda_inspections/inter-bio-lab-inc/d8d51445-e689-4e51-afd1-6f7b55ed7c4b
Source feed: FDA_Inspections

> FDA inspection 1112335 of Inter Bio-Lab, Inc., December 05, 2019. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1112335
- Company Name: Inter Bio-Lab, Inc.
- Inspection Date: 2019-12-05
- 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

Company: https://www.keypedia.com/companies/inter-bio-lab-inc/10e3dea8-4824-4655-bd9c-c3e537dffc9e

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