FDA Inspection
Newman Lasik Centers, LLCNewman Lasik Centers, LLC – FDA Inspection, Aug 8, 2011
Record Details
This FDA Inspection record concerns Newman Lasik Centers, LLC, with an inspection on August 8, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Newman Lasik Centers, LLC
- Inspection Date
- August 8, 2011
- Product Type
- Devices
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ID · eb94f30e-48a8-468a-a54e-da6e371b8dc5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 739121
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
1- 21 CFR 803.17Lack of Written MDR Procedures
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