# Frontida BioPharm Inc – FDA Inspection, Jul 19, 2019

Source: https://www.keypedia.com/records/fda_inspections/frontida-biopharm-inc/19fa9164-4fb0-41e4-9013-e9731116e4ad
Source feed: FDA_Inspections

> FDA inspection 1097023 of Frontida BioPharm Inc, July 19, 2019. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 211. Form 483 issued. 14 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1097023
- Company Name: Frontida BioPharm Inc
- Inspection Date: 2019-07-19
- 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: 1

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## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jaison-j-eapen/35b16029-11a0-452c-9413-a92dc120c529)
- [Company Rep](https://www.keypedia.com/people/michael-l-casner/a0f35f37-4795-4edf-a9f6-a447d64c0fd4)

Company: https://www.keypedia.com/companies/frontida-biopharm-inc/dc8190f9-0e13-4160-a611-dcf664f43b09

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