FDA Form 483s for Iotamotion, Randy Hicks, Life Sciences Vandalia, DDC Technologies, and Strata Skin Sciences

FDA Form 483s for Iotamotion, Randy Hicks, Life Sciences Vandalia, DDC Technologies, and Strata Skin Sciences

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Original Request: Please provide the following inspection-related document(s) in electronic PDF format related to product type Devices: The 483(s) (in electronic format) for the inspection of Iotamotion Inc (FEI 3021286080), located in Vadnais Heights, Minnesota, United States, inspection ending 2024-09-12. The 483(s) (in electronic format) for the inspection of Randy D. Hicks, M.D. (FEI 3031511465), located in Flint, Michigan, United States, inspection ending 2024-09-12. The 483(s) (in electronic format) for the inspection of Life Sciences Vandalia (FEI 1000200989), located in Dayton, Ohio, United States, inspection ending 2024-09-06. The 483(s) (in electronic format) for the inspection of DDC Technologies, Inc. (FEI 3002757272), located in Oceanside, New York, United States, inspection ending 2024-09-06. The 483(s) (in electronic format) for the inspection of Strata Skin Sciences, Inc. (FEI 3002942014), located in Carlsbad, California, United States, inspection ending 2024-08-22.
Tags: MedTech, 483, 2024
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.

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