# FDA Inspection 1272017 - Techpharm GmbH - February 23, 2023

Source: https://www.keypedia.com/records/fda_inspections/techpharm-gmbh/b9b35044-a6e1-4a29-bea5-bc0edca919b3
Source feed: FDA_Inspections

> FDA Inspection 1272017 for Techpharm GmbH on February 23, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1272017
- Company Name: Techpharm GmbH
- Inspection Date: 2023-02-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

## Related Documents

- [FDA Inspection 1044988 - 2018-02-09](https://www.keypedia.com/records/fda_inspections/techpharm-gmbh/200f01a0-531e-40d9-b926-67782a575db5)
- [FDA Inspection 853425 - 2013-09-23](https://www.keypedia.com/records/fda_inspections/techpharm-gmbh/c8932e74-7a75-4d05-927a-f011e3af9211)

Company: https://www.keypedia.com/companies/techpharm-gmbh/9083f8fd-d4e0-4644-a664-44d187e2df7d

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