FDA Inspection
Zimmer Surgical IncZimmer Surgical Inc – FDA Inspection, May 23, 2016
Record Details
This FDA Inspection record concerns Zimmer Surgical Inc, with an inspection on May 23, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Zimmer Surgical Inc
- Inspection Date
- May 23, 2016
- Product Type
- Devices
View Company Profile
ID · 54f17391-6c12-42de-a144-15d17837c89c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 973469
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
4- 21 CFR 820.100(b)Documentation
- 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 820.198(e)Records of complaint investigation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Zimmer Surgical Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 21, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 21, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Zimmer Surgical Inc
- FDA Inspection 832719 - 2013-05-21
- FDA Inspection 756260 - 2011-10-21
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