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EIR
•1RUWK $PHULFDQ 6FLHQFH $VVRFLDWHV ,QF•August 16, 2018

1RUWK $PHULFDQ 6FLHQFH $VVRFLDWHV ,QF – FDA EIR, Aug 16, 2018

Record Details

A routine FDA inspection was conducted at North American Science Associates, Inc. (NAMSA) in Northwood, OH, from August 13 to August 16, 2018. This pre-announced inspection was performed under Compliance Program 7348.808, focusing on Good Laboratory Practice (Nonclinical Laboratories) to ensure adherence to regulatory frameworks like 21 CFR Part 58. The scope included a comprehensive review of facilities, operations, quality assurance, personnel, equipment, test article accountability, standard operating procedures, and the conduct of three specific nonclinical studies. Notably, the inspection concluded without identifying any main violations or objectionable conditions. As a result, no FDA Form 483, List of Inspectional Observations, was issued to NAMSA, and no refusals were encountered or samples collected. Consequently, no specific regulatory actions or voluntary corrections were required by the FDA following this inspection, indicating that the facility was found to be in compliance with applicable regulations.

Company
1RUWK $PHULFDQ 6FLHQFH $VVRFLDWHV ,QF
Inspection date
August 16, 2018
Product type
devices
Office
Food and Drug Administration
People
  • Kathryn L. Suttling (issuing_officer)
  • Mark Shumaker (company_representative)
  • Jean Pierre Boutrand (company_representative)
  • John J. Gorski (recipient)
  • Marcia A. Worley (investigator)
View Company Profile

ID · 5eac22b4-3c2a-4043-b7c3-4bd8509c3e29

Violation Codes3
21 CFR 58.8121 CFR 58.12021 CFR 58.185

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