# FDA Inspection 1052621 - Bioflo LLC - May 15, 2018

Source: https://www.keypedia.com/records/fda_inspections/bioflo-llc/b43fb8e5-9bf7-4ea6-9b97-976ce226875e
Source feed: FDA_Inspections

> FDA Inspection 1052621 for Bioflo LLC on May 15, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1052621
- Company Name: Bioflo LLC
- Inspection Date: 2018-05-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1052621 - 2018-05-15](https://www.keypedia.com/records/fda_inspections/bioflo-llc/5a3c485e-e62c-4134-8ed1-e745d6ab176a)

Company: https://www.keypedia.com/companies/bioflo-llc/f84c33e0-98e5-4641-89ad-0819678add27

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