FDA Inspection
Molecular Products, Ltd.Molecular Products, Ltd. – FDA Inspection, Feb 14, 2019
Record Details
This FDA Inspection record concerns Molecular Products, Ltd., with an inspection on February 14, 2019, issued by the Center for Devices and Radiological Health, covering devices.
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ID · d8f20e52-a06f-410f-a1a9-a3e5e588cf50
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1079981
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.80(d)Lack of or inadequate final acceptance procedures
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
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