# FDA Inspection 1100901 - Bioforce AG - August 23, 2019

Source: https://www.keypedia.com/records/fda_inspections/bioforce-ag/94f999ba-dcd1-4fae-bcb0-82d7f8db36c0
Source feed: FDA_Inspections

> FDA Inspection 1100901 for Bioforce AG on August 23, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1100901
- Company Name: Bioforce AG
- Inspection Date: 2019-08-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

Company: https://www.keypedia.com/companies/bioforce-ag/24591383-7b30-4b6d-9c44-2cb66d15d52e

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