FDA Inspection
Kevin Waltz, OD, MDKevin Waltz, OD, MD – FDA Inspection, May 23, 2012
Record Details
This FDA Inspection record concerns Kevin Waltz, OD, MD, with an inspection on May 23, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Kevin Waltz, OD, MD
- Inspection Date
- May 23, 2012
- Product Type
- Devices
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ID · 1624193a-51ea-4829-952e-f390a16f4eab
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 784218
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 312.60FD-1572, protocol compliance
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Other FDA inspections of Kevin Waltz, OD, MD
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 17, 2016 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| September 20, 2013 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Kevin Waltz, OD, MD
- FDA Inspection 972327 - 2016-05-17
- FDA Inspection 849797 - 2013-09-20
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