FDA Inspection
Cavalier ALP, LLC dba Currie Medical SpecialtiesCavalier ALP, LLC dba Currie Medical Specialties – FDA Inspection, Jul 11, 2019
Record Details
This FDA Inspection record concerns Cavalier ALP, LLC dba Currie Medical Specialties, with an inspection on July 11, 2019, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- July 11, 2019
- Product Type
- Devices
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ID · 82ee03bf-5e2c-4321-88de-79e93b5508c6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1096552
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
5- 21 CFR 820.75(a)Lack of or inadequate process validation
- 21 CFR 820.70(g)(2)Periodic equipment inspections
- 21 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
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Other FDA inspections of Cavalier ALP, LLC dba Currie Medical Specialties
2| Date | Classification | Office | Project area |
|---|---|---|---|
| March 30, 2026 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| December 16, 2022 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Cavalier ALP, LLC dba Currie Medical Specialties
- FDA Inspection 1311784 - 2026-03-30
- FDA Inspection 1193745 - 2022-12-16
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