# FDA Inspection 1026870 - OMNILIFE USA, Inc. dba Texas OMNILIFE USA, Inc. - September 08, 2017

Source: https://www.keypedia.com/records/fda_inspections/omnilife-usa-inc-dba-texas-omnilife-usa-inc/9e218fe2-4dba-4879-8b72-18c85679f8e8
Source feed: FDA_Inspections

> FDA Inspection 1026870 for OMNILIFE USA, Inc. dba Texas OMNILIFE USA, Inc. on September 08, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026870
- Company Name: OMNILIFE USA, Inc. dba Texas OMNILIFE USA, Inc.
- Inspection Date: 2017-09-08
- Classification: No Action Indicated (NAI)
- Project Area: Foodborne Biological Hazards
- Product Type: Food/Cosmetics
- Office Name: Center for Food Safety and Applied Nutrition

## Related Documents

- [FDA Inspection 1204464 - 2023-04-28](https://www.keypedia.com/records/fda_inspections/omnilife-usa-inc-dba-texas-omnilife-usa-inc/f4927db4-05ae-4562-8290-577a4934aaef)

Company: https://www.keypedia.com/companies/omnilife-usa-inc-dba-texas-omnilife-usa-inc/0bf756c9-7f43-4b3e-a47e-820d4ab10eff

Office: https://www.keypedia.com/offices/center-for-food-safety-and-applied-nutrition/e04dc4e5-ee4f-4b0d-be8c-1139531ddab2