# BodyBio Inc. - Inspection Records

Source: https://www.keypedia.com/companies/bodybio-inc/6452e0be-b03e-4cf3-82c4-2bdb8e41df7d

> Inspection records and compliance data for BodyBio Inc. in Millville, New Jersey. Access full analysis and detailed observations.

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## Details

- Name: BodyBio Inc.
- FEI Number: 3003638959
- City: Millville
- State: New Jersey
- Country Name: United States
- Address Line 1: 45 Reese Rd
- Zip Code: 08332

## Related Documents

- [FDA Inspection 1292888 - BodyBio Inc. - 2025-10-30](https://www.keypedia.com/records/fda_inspections/bodybio-inc/0c7f54ff-c11c-4699-b73b-1c099c98764e) — classification: No Action Indicated (NAI), source: FDA, date: October 30, 2025
- [FDA Inspection 1237109 - BodyBio Inc. - 2024-04-26](https://www.keypedia.com/records/fda_inspections/bodybio-inc/257c5788-bd28-4406-880c-6e6d4c341553) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 26, 2024
- [FDA Inspection 1086637 - BodyBio Inc. - 2019-04-18](https://www.keypedia.com/records/fda_inspections/bodybio-inc/c73b3584-2d6f-4422-bf74-d875847d29e0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 18, 2019
- [FDA Inspection 1086637 - BodyBio Inc. - 2019-04-18](https://www.keypedia.com/records/fda_inspections/bodybio-inc/c72470d3-ecab-44ef-8cb5-d7875223caad) — classification: No Action Indicated (NAI), source: FDA, date: April 18, 2019
- [FDA Inspection 996675 - BodyBio Inc. - 2016-11-29](https://www.keypedia.com/records/fda_inspections/bodybio-inc/7d489916-a77e-4734-964d-2956469c0956) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 29, 2016
- [FDA Inspection 853026 - BodyBio Inc. - 2013-10-30](https://www.keypedia.com/records/fda_inspections/bodybio-inc/efab5b76-bf38-4254-82df-a3de754c9e31) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 30, 2013
- [FDA Inspection 610352 - BodyBio Inc. - 2009-09-04](https://www.keypedia.com/records/fda_inspections/bodybio-inc/c20fbb0a-7892-4f33-93d1-2f20cd85830b) — classification: No Action Indicated (NAI), source: FDA, date: September 4, 2009

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