FDA Inspection
MW Life Sciences - MansfieldMW Life Sciences - Mansfield – FDA Inspection, Sep 17, 2014
Record Details
This FDA Inspection record concerns MW Life Sciences - Mansfield, with an inspection on September 17, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- MW Life Sciences - Mansfield
- Inspection Date
- September 17, 2014
- Product Type
- Devices
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ID · ba1d6d73-29a3-48f2-a977-6be63f74e7d2
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 894259
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.90(b)(1)Procedures for product review,disposition lack of/inadequate
- 21 CFR 820.75(a)Documentation
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Other FDA inspections of MW Life Sciences - Mansfield
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 25, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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