FDA Inspection
John Lane, MDJohn Lane, MD – FDA Inspection, Jul 26, 2016
Record Details
This FDA Inspection record concerns John Lane, MD, with an inspection on July 26, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- John Lane, MD
- Inspection Date
- July 26, 2016
- Product Type
- Devices
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ID · 7a863740-65ac-493e-bc61-f160b0911f1e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 979026
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.140(a)(3)(ii)Investigator records of relevant observations inadequate
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