# FDA Inspection 618021 - Probactive Biotech, Inc. dba St. Paul Brands - July 16, 2009

Source: https://www.keypedia.com/records/fda_inspections/probactive-biotech-inc-dba-st-paul-brands/6de0280b-b684-49ae-9577-03a6e5a12f31
Source feed: FDA_Inspections

> FDA Inspection 618021 for Probactive Biotech, Inc. dba St. Paul Brands on July 16, 2009. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 618021
- Company Name: Probactive Biotech, Inc. dba St. Paul Brands
- Inspection Date: 2009-07-16
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 805468 - 2012-10-19](https://www.keypedia.com/records/fda_inspections/probactive-biotech-inc-dba-st-paul-brands/208257dc-67d0-4a01-84fa-9b69f4e55a5e)
- [FDA Inspection 618021 - 2009-07-16](https://www.keypedia.com/records/fda_inspections/probactive-biotech-inc-dba-st-paul-brands/bcdd6636-82a0-4a1c-a059-9eb7f9299503)
- [FDA Inspection 614494 - 2009-07-15](https://www.keypedia.com/records/fda_inspections/probactive-biotech-inc-dba-st-paul-brands/63abb979-27de-4301-bb04-be6d7798eda7)

Company: https://www.keypedia.com/companies/probactive-biotech-inc-dba-st-paul-brands/81d55082-1f56-4b06-8c87-72a09ee6f0b4

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