# FDA Inspection 1060828 - Helixor Heilmittel GmbH - July 13, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/helixor-heilmittel-gmbh/d438d10e-729b-4d7c-820f-777f05bef1fc
Source feed: FDA_Inspections

> FDA Inspection 1060828 for Helixor Heilmittel GmbH on July 13, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1060828
- Company Name: Helixor Heilmittel GmbH
- Inspection Date: 2018-07-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

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Company: https://www.globalkeysolutions.net/companies/helixor-heilmittel-gmbh/b45b37c5-5091-40fb-9f4b-7079f034af6d

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