FDA Inspection
Sanford Laboratories Fargo RegionSanford Laboratories Fargo Region – FDA Inspection, Apr 11, 2013
Record Details
This FDA Inspection record concerns Sanford Laboratories Fargo Region, with an inspection on April 11, 2013, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- April 11, 2013
- Product Type
- Biologics
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ID · 51630c3b-69a6-4a0d-926f-73ce89ce04c3
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 826835
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
1- 21 CFR 606.170(b)Adverse reaction - fatality
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Other FDA inspections of Sanford Laboratories Fargo Region
5| Date | Classification | Office | Project area |
|---|---|---|---|
| May 1, 2025 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| May 28, 2019 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| December 13, 2016 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| November 19, 2014 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| February 28, 2012 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Sanford Laboratories Fargo Region
- FDA Inspection 1272472 - 2025-05-01
- FDA Inspection 1094250 - 2019-05-28
- FDA Inspection 995143 - 2016-12-13
- FDA Inspection 904556 - 2014-11-19
- FDA Inspection 770001 - 2012-02-28
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