FDA Inspection
Wasserburger Arzneimittelwerk GmbHFDA Inspection 1039842 - Wasserburger Arzneimittelwerk GmbH - January 23, 2018
Record Details
This FDA Inspection record concerns Wasserburger Arzneimittelwerk GmbH, with an inspection on January 23, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- January 23, 2018
- Product Type
- Drugs
View Company Profile
ID · 70fc24d5-ea46-45dc-ae8c-1c19e78239d7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1039842
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
2- 21 CFR 211.67(a)Cleaning / Sanitizing / Maintenance
- 21 CFR 211.194(a)(4)Complete Test Data
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Wasserburger Arzneimittelwerk GmbH
4| Date | Classification | Office | Project area |
|---|---|---|---|
| May 2, 2024 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| October 27, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 10, 2013 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 9, 2010 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Wasserburger Arzneimittelwerk GmbH
- FDA Inspection 1240649 - 2024-05-02
- FDA Inspection 947759 - 2015-10-27
- FDA Inspection 852201 - 2013-09-10
- FDA Inspection 703289 - 2010-11-09
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.