FDA Inspection
Bioiberica, SAUBioiberica, SAU – FDA Inspection, Sep 21, 2018
Record Details
This FDA Inspection record concerns Bioiberica, SAU, with an inspection on September 21, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.
View Company Profile
ID · 29477487-86b8-4f8f-b5fa-0b46e5a68705
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1068320
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Bioiberica, SAU
7| Date | Classification | Office | Project area |
|---|---|---|---|
| September 20, 2024 | Not classified | Office of Inspections and Investigations | |
| February 4, 2022 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 17, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 23, 2017 | Not classified | Office of Inspections and Investigations | |
| May 28, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Bioiberica, SAU
- FDA Inspection 1253863 - 2024-09-20
- FDA Inspection 1162922 - 2022-02-04
- FDA Inspection 1127299 - 2019-12-17
- FDA Inspection 1018467 - 2017-03-23
- FDA Inspection 932850 - 2015-05-28
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.