# FDA Inspection 1112335 - Inter Bio-Lab, Inc. - December 05, 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 for Inter Bio-Lab, Inc. on December 05, 2019. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1112335 - 2019-12-05](https://www.keypedia.com/records/fda_inspections/inter-bio-lab-inc/d87d7084-93d4-42f7-9cfe-d2b6822cd0c9)

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