FDA Inspection
Melissas Enterprises of Madison IncMelissas Enterprises of Madison Inc – FDA Inspection, Nov 4, 2013
Record Details
This FDA Inspection record concerns Melissas Enterprises of Madison Inc, with an inspection on November 4, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- November 4, 2013
- Product Type
- Devices
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ID · cb25129b-b0f4-41fc-a2f3-b755e0f9fbf6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 854257
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
- 21 CFR 803.17Lack of Written MDR Procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Melissas Enterprises of Madison Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 9, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| December 13, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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