# FDA Inspection 977719 - Bio Protech, Inc. - March 23, 2016

Source: https://www.keypedia.com/records/fda_inspections/bio-protech-inc/b7782e43-d2a0-4d98-bf17-34a6c6f1a40f
Source feed: FDA_Inspections

> FDA Inspection 977719 for Bio Protech, Inc. on March 23, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 977719
- Company Name: Bio Protech, Inc.
- Inspection Date: 2016-03-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 977719 - 2016-03-23](https://www.keypedia.com/records/fda_inspections/bio-protech-inc/ac9789da-231d-465e-a2e0-a000ba717aab)
- [FDA Inspection 704336 - 2010-12-09](https://www.keypedia.com/records/fda_inspections/bio-protech-inc/57b6546f-2b2e-4501-b2e0-b3a80ba4e4b0)
- [FDA Inspection 704336 - 2010-12-09](https://www.keypedia.com/records/fda_inspections/bio-protech-inc/0b1216a1-5f8f-4839-8483-a486abe3a3b9)

Company: https://www.keypedia.com/companies/bio-protech-inc/6be640bc-59c4-4c6d-aa5b-a4c13a1e99f9

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