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OTI received a warning letter in connection with a FDA
sec.edgar-online.com (Aug 12 2008) Ophthalmology Explore Article
On March 25, 2008, OTI received a warning letter in connection with a FDA inspection of OTI's facilities in July and August of 2007. The warning letter cited several deficiencies in OTI's quality, record keeping, and reporting systems relating to certain of OTI's products, including the OTI Scan 1000, OTI Scan 2000, and OTI OCT/SLO combination imaging system. Based upon the observations noted in the warning letter, OTI is not ... (Read Full Article)
Comment on Article Mentions: OPKO Health Ophthalmic Technologies OCT/SLO OTI Ophthalmic Technologies Inc.






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