# Weleda AG – FDA Inspection, Jun 15, 2018

Source: https://www.keypedia.com/records/fda_inspections/weleda-ag/4af970c0-a255-4c1a-a7c5-25620c393201
Source feed: FDA_Inspections

> FDA inspection 1061389 of Weleda AG, June 15, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1061389
- Company Name: Weleda AG
- Inspection Date: 2018-06-15
- 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: 0

## Related Documents

- FDA Inspection 1290150 - 2024-07-17
- FDA Inspection 1154630 - 2019-11-21
- FDA Inspection 978925 - 2016-06-10
- [FDA Inspection 794146 - 2012-04-12](https://www.keypedia.com/records/fda_inspections/weleda-ag/8523940b-b00c-436c-8e08-7063620b25e0)
- FDA Inspection 776626 - 2012-03-13

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/christopher-r-czajka/42defbf3-ea06-4090-8d51-7da2b07d9e84)
- Issuing Officer

Company: https://www.keypedia.com/companies/weleda-ag/98031034-9280-418f-9f50-55223de9bf84

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