FDA Investigator: Kimetha A. King

- Kimetha A. King first started conducting FDA inspections in 2006, with the last inspection in 2010. Over that time, Kimetha A. King has conducted 44 inspections at 43 companies across 43 sites.

Get Kimetha King's official FDA inspection documents. Gain valuable insights from their Form 483s and EIRs to ace your next inspection.

Documents

Upon purchase, you will receive an email with a link to immediately download the documents.

FDA 483 BioFire Diagnostics, Inc., Salt Lake City | 2010

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Kimetha A. King
Medical Devices & Rad Health Form 483

FDA 483 Novocol, Inc., Louisville | 2010

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Kimetha A. King
Human Drug Form 483

FDA 483 nSpire Health, Inc., Longmont | 2010

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Kimetha A. King
Medical Devices & Rad Health Form 483

FDA 483 Encision Inc., Boulder | 2009

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Kimetha A. King
Medical Devices & Rad Health Form 483

FDA 483 Shippert Medical Technologies, Centennial | 2009

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Kimetha A. King
Medical Devices & Rad Health Form 483

FDA 483 Avanca Medical Devices, Albuquerque | 2009

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Kimetha A. King
Medical Devices & Rad Health Form 483

FDA 483 ARCA biopharma, Inc., Broomfield | 2009

Out-of-stock
Kimetha A. King
Human Drug Form 483