FDA Inspection
Wyeth Lederle S.r.lWyeth Lederle S.r.l – FDA Inspection, Jul 20, 2012
Record Details
This FDA Inspection record concerns Wyeth Lederle S.r.l, with an inspection on July 20, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Wyeth Lederle S.r.l
- Inspection Date
- July 20, 2012
- Product Type
- Drugs
View Company Profile
ID · dc444967-e078-4b26-8b17-8010b6d7751b
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 792624
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Wyeth Lederle S.r.l
4| Date | Classification | Office | Project area |
|---|---|---|---|
| January 21, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 20, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 14, 2014 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 4, 2009 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Wyeth Lederle S.r.l
- FDA Inspection 1178127 - 2022-01-21
- FDA Inspection 1012188 - 2017-04-20
- FDA Inspection 903600 - 2014-11-14
- FDA Inspection 637083 - 2009-12-04
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.