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483
•Trigen Laboratories•November 15, 2019

Trigen Laboratories – FDA 483, Nov 15, 2019

Record Details

An FDA inspection of Trigen Laboratories, Inc. in Tampa, FL, a medical device manufacturer, revealed significant deficiencies in their quality system. The firm lacked adequate written procedures for handling customer complaints, managing Medical Device Reportable events, and controlling purchased products and services from suppliers. These issues indicate a failure to establish and maintain essential quality controls for medical device manufacturing.

Company
Trigen Laboratories
Inspection date
November 15, 2019
Product type
device
Office
Office of Medical Device and Radiological Health Division II
Person
  • Joshua J. Silvestri
View Company Profile

ID · a2675243-e065-4100-ba46-e3e0434a1add

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Contact
New York Office:
370 Jay Street 7th Floor
Brooklyn, NY 11201
Scranton Office:
Scranton Enterprise Center, Suite 217
201 Lackawanna Avenue
Scranton, PA, 18503
🇺🇸+1 917-789-5099
🇪🇺+48 532-447-507
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