FDA Inspection
Fidelio Healthcare Limburg GmbHFidelio Healthcare Limburg GmbH – FDA Inspection, Feb 2, 2017
Record Details
This FDA Inspection record concerns Fidelio Healthcare Limburg GmbH, with an inspection on February 2, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
View Company Profile
ID · ce68abde-899e-486f-87c8-c9710652eb03
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 999720
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Fidelio Healthcare Limburg GmbH
4| Date | Classification | Office | Project area |
|---|---|---|---|
| November 17, 2023 | Not classified | Office of Inspections and Investigations | |
| July 20, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 23, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 21, 2011 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Fidelio Healthcare Limburg GmbH
- FDA Inspection 1223517 - 2023-11-17
- FDA Inspection 1234400 - 2022-07-20
- FDA Inspection 889394 - 2014-05-23
- FDA Inspection 748702 - 2011-09-21
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.