FDA Inspection 1136643 — Clariant Produkte (Deutschland) GmbH
The FDA completed an inspection of Clariant Produkte (Deutschland) GmbH on June 24, 2020 in Burgkirchen A.D.Alz. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- June 24, 2020
- Fiscal Year
- 2020
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Burgkirchen A.D.Alz (Germany)
Additional Details
Mutual Recognition Agreement (MRA)