FDA Inspection
CenexiCenexi – FDA Inspection, May 13, 2016
Record Details
This FDA Inspection record concerns Cenexi, with an inspection on May 13, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Cenexi
- Inspection Date
- May 13, 2016
- Product Type
- Drugs
View Company Profile
ID · e965d5ae-4201-41b8-98b4-7e6b477a42f9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 973211
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
1- 21 CFR 211.198(a)Adverse Drug Experience
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Cenexi
3| Date | Classification | Office | Project area |
|---|---|---|---|
| December 14, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 12, 2016 | VAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
| May 7, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Cenexi
- FDA Inspection 1243938 - 2022-12-14
- FDA Inspection 990472 - 2016-07-12
- FDA Inspection 668589 - 2010-05-07
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.