# FDA 483 - Bio-Recovery Inc. - July 24, 2018

Source: https://www.globalkeysolutions.net/records/483/bio-recovery-inc/5b235241-2837-4725-acd1-bfc68e053917

> FDA 483 for Bio-Recovery Inc. on July 24, 2018. Product: other. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Bio-Recovery Inc.
- Inspection Date: 2018-07-24
- Product Type: other
- Office Name: Minneapolis District Office
- Summary: An FDA inspection of Bio-Recovery Inc., an own label distributor in Minneapolis, MN, revealed significant quality control deficiencies. The firm failed to properly review documentation for quarantined products and did not conduct necessary tests for strength and contamination before releasing dietary supplements. These issues indicate a lack of adherence to established specifications and testing requirements for product release.

## Related Documents

- [WARNING_LETTER - 2013-05-17](https://www.globalkeysolutions.net/records/warning_letter/bio-recovery-inc/72f21d8d-8b60-4913-a4be-b08cdbc3e559)

## Related Officers

- [Douglas J. Snyder](https://www.globalkeysolutions.net/people/douglas-j-snyder/d4fcec9d-230d-4481-a5e5-8ef7d0dbfdd2)

Company: https://www.globalkeysolutions.net/companies/bio-recovery-inc/56d3aeff-acbe-4836-aeb9-30814a4eb4c1

Office: https://www.globalkeysolutions.net/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d