FDA Inspection
Longport, IncLongport, Inc – FDA Inspection, Sep 21, 2010
Record Details
This FDA Inspection record concerns Longport, Inc, with an inspection on September 21, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Longport, Inc
- Inspection Date
- September 21, 2010
- Product Type
- Devices
View Company Profile
ID · b90a8c07-6283-4a5f-89eb-77fd594a00f9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 681275
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
4- 21 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.20(e)Quality System Procedures
- 21 CFR 820.20(a)Quality policy and objectives
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