FDA EIR & 483 – Klocke of America Inc. (PDMA Inspection – Mar 2022)

FDA EIR & 483 – Klocke of America Inc. (PDMA Inspection – Mar 2022)

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Original Request: a Freedom of Information Act request for any and all Establishment Inspection Reports and 483 Forms related to the following inspection conducted pursuant to the Prescription Drug Marketing Act (“PDMA”): Inspection Date: 3/30/2022 Entity Name & Address: Klocke of America, Inc. 14201 Jetport Loop W Fort Myers, FL 33913-7713
  • 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. Learn more about Fast-Track Requests here.

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