FDA Inspection
Orthority CorporationOrthority Corporation – FDA Inspection, Mar 27, 2012
Record Details
This FDA Inspection record concerns Orthority Corporation, with an inspection on March 27, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Orthority Corporation
- Inspection Date
- March 27, 2012
- Product Type
- Devices
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ID · aefd06f0-b84a-450c-8db7-1ec0b85e4151
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 774189
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 1271.200(b)Procedures inadequate
- 21 CFR 820.150Lack of or inadequate procedures for storage.
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Other FDA inspections of Orthority Corporation
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 8, 2022 | NAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
| August 14, 2018 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| July 9, 2015 | VAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Orthority Corporation
- FDA Inspection 1162402 - 2022-02-08
- FDA Inspection 1064451 - 2018-08-14
- FDA Inspection 935460 - 2015-07-09
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