# FDA Inspection 917610 - Ultra ZX Labs, LLC - March 13, 2015

Source: https://www.keypedia.com/records/fda_inspections/ultra-zx-labs-llc/74850abb-4b63-4dbd-a14f-3b60c19bb6e1
Source feed: FDA_Inspections

> FDA Inspection 917610 for Ultra ZX Labs, LLC on March 13, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 917610
- Company Name: Ultra ZX Labs, LLC
- Inspection Date: 2015-03-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Unapproved and Misbranded Drugs
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

## Related Documents

- [FDA Inspection 917610 - 2015-03-13](https://www.keypedia.com/records/fda_inspections/ultra-zx-labs-llc/c7a06fbb-be1f-4b11-97f1-d831469fdb3b)

Company: https://www.keypedia.com/companies/ultra-zx-labs-llc/b1f8284e-49f8-4b97-9d70-77a726c6120a

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c