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FDA Inspection
•Navinta, LLC•September 18, 2018

Navinta, LLC – FDA Inspection, Sep 18, 2018

Record Details

This FDA Inspection record concerns Navinta, LLC, with an inspection on September 18, 2018, issued by the New Jersey District Office, covering human drugs.

Company
Navinta, LLC
Inspection Date
September 18, 2018
Product Type
Human Drugs
Office
New Jersey District Office
Person
  • James R. Birkenstamm (Issuing Officer)
View Company Profile

ID · 89d9cbd4-879b-471f-8a04-efacf0821bff

Inspection Facts

Inspection number
1070302
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Navinta, LLC

7
DateClassificationOfficeProject area
September 30, 2024Not classifiedNew Jersey District Office
June 29, 2023Not classifiedNew Jersey District Office
May 4, 2023NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
March 28, 2019VAICenter for Drug Evaluation and ResearchBioresearch Monitoring
August 18, 2017VAICenter for Drug Evaluation and ResearchPostmarket Surv. and Epidemiology
View all 7 other inspections on the company page
Other documents for Navinta, LLC
  • FDA Inspection 1252822 - 2024-09-30
  • FDA Inspection 1209856 - 2023-06-29
  • FDA Inspection 1205480 - 2023-05-04
  • FDA Inspection 1084188 - 2019-03-28
  • FDA Inspection 1022105 - 2017-08-18

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Contact
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Brooklyn, NY 11201
Scranton Office:
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