Kunimoto, M.D., Derek Y. – FDA EIR, Apr 8, 2009

An FDA inspection was conducted at Derek Y. Kunimoto, M.D., located in Phoenix, AZ, spanning from March 25, 2009, to April 8, 2009. The inspection was carried out by FDA Investigators Timothy T Kapsala and Diana L. Ayala. While the administrative details of the inspection, including the establishment's FEI number (3007392097) and the dates of the review, are present, the critical substantive content of the inspection report is extensively redacted. Specifically, the document does not provide any information regarding the main violations or issues discovered during this regulatory assessment. The sections typically detailing observed deficiencies, non-compliance, or areas requiring improvement are marked as 'b (4)' or 'b (6)', indicating that this information has been withheld. As a result, it is impossible to ascertain the specific regulatory framework or statutes that may have been violated. Furthermore, any required actions, corrective measures, or recommendations issued to Derek Y. Kunimoto, M.D. following the inspection are also not disclosed within the provided text, making it impossible to summarize the outcomes or next steps of this FDA inspection.