# Ultrum Labs LLC – FDA Inspection, Oct 16, 2023

Source: https://www.keypedia.com/records/fda_inspections/ultrum-labs-llc/c4f304d7-f531-4e1e-bf90-779e36548361
Source feed: FDA_Inspections

> FDA inspection 1220528 of Ultrum Labs LLC, October 16, 2023. Classification: Voluntary Action Indicated (VAI). 12 citations under 21 CFR part 211. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1220528
- Company Name: Ultrum Labs LLC
- Inspection Date: 2023-10-16
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 12

## Related Officers

- [Investigator](https://www.keypedia.com/people/damaris-y-hernandez/ca16093e-047b-4bf1-bcc1-c439cff21e8a)
- [FDA Associated Person](https://www.keypedia.com/people/nicole-e-knowlton/8e65400f-249f-45fe-96fc-cb00fec6ae39)

Company: https://www.keypedia.com/companies/ultrum-labs-llc/55b122bd-b18f-429a-99fa-991470ec9e90

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