# Regenesis Biomedical Inc – FDA Inspection, May 16, 2017

Source: https://www.keypedia.com/records/fda_inspections/regenesis-biomedical-inc/30fb3abc-44d9-4324-a32c-ea49ba85e833
Source feed: FDA_Inspections

> FDA inspection 1024124 of Regenesis Biomedical Inc, May 16, 2017. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024124
- Company Name: Regenesis Biomedical Inc
- Inspection Date: 2017-05-16
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 838831 - 2013-06-11
- FDA Inspection 752842 - 2011-11-09
- FDA Inspection 599980 - 2009-07-20

## Related Officers

- [Company Rep](https://www.keypedia.com/people/charles-l-larson/4232255d-bfd6-4616-a854-c801e4c23e1c)

Company: https://www.keypedia.com/companies/regenesis-biomedical-inc/fa5bdc45-63c5-4b6d-b39b-03bbc74019fa

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