# FDA Inspection 1063135 - Omnia Biologix, LLC - July 10, 2018

Source: https://www.keypedia.com/records/fda_inspections/omnia-biologix-llc/2f2a90df-69b3-4ae4-a9b9-b2ad17cabbde
Source feed: FDA_Inspections

> FDA Inspection 1063135 for Omnia Biologix, LLC on July 10, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1063135
- Company Name: Omnia Biologix, LLC
- Inspection Date: 2018-07-10
- Classification: No Action Indicated (NAI)
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

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Company: https://www.keypedia.com/companies/omnia-biologix-llc/7d7569ca-0d21-48cd-ac98-5a4ff2fc61b5

Office: https://www.keypedia.com/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d