# FDA Inspection 1101333 - Reprobiotech Corp - September 05, 2019

Source: https://www.keypedia.com/records/fda_inspections/reprobiotech-corp/e364714c-7c23-4b10-9bf7-80b1cf18040e
Source feed: FDA_Inspections

> FDA Inspection 1101333 for Reprobiotech Corp on September 05, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1101333
- Company Name: Reprobiotech Corp
- Inspection Date: 2019-09-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/reprobiotech-corp/2a7115f6-b546-4451-997a-734406e0c998

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