FDA Inspection
Mississippi Fertility InstituteMississippi Fertility Institute – FDA Inspection, May 3, 2010
Record Details
This FDA Inspection record concerns Mississippi Fertility Institute, with an inspection on May 3, 2010, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- May 3, 2010
- Product Type
- Biologics
View Company Profile
ID · 342d791f-a30f-4b76-8fd2-03ff3af5984e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 663950
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
8- 21 CFR 1271.55(d)(1)Documentation maintained (general)
- 21 CFR 1271.75(a)(1)Risk factors, clinical evidence
- 21 CFR 1271.50(a)Determination based on screening and testing
- 21 CFR 1271.90(c)Eligibility not required--warning labels
- 21 CFR 1271.47(a)Procedures for all other requirements
- 21 CFR 1271.55(b)(2)Listing and interpretation of CD tests performed
- 21 CFR 1271.55(b)(1)Statement re: certified testing lab
- 21 CFR 1271.55(b)(3)Name and address on summary
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Mississippi Fertility Institute
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 12, 2015 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| June 19, 2012 | VAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Mississippi Fertility Institute
- FDA Inspection 912231 - 2015-01-12
- FDA Inspection 787326 - 2012-06-19
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.