Productora Clinimex Industrial S A De C V

FDA Filings

This page includes the latest FDA filings for Productora Clinimex Industrial S A De C V. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3008860832
• FEI Number: 3008860832
• Name: PRODUCTORA CLINIMEX INDUSTRIAL S.A. DE C.V.
• Owner & Operator: PRODUCTORA CLINIMEX INDUSTRIAL S.A. DE C.V.
• Contact Address: Panamericana 202-B Jesus Gomez Portugal, Jesus Maria; Aquascalientes MX-AGU Aguascalientes 20909 MX
• Official Correspondent:
  • ALFREDO PONTON
  • 52-449-9730302-x
• US Agent:
  • Jeff Lennon
  • AMD Medicom Inc.
  • 706 2070574
  • Jlennon@amdritmed.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: Panamericana 202-B Jesus Gomez Portugal, Jesus Maria; Aquascalientes Aguascalientes, 20909 MX
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
OEA PRODUCTORA CLINIMEX INDUSTRIAL S.A. DE C.V.	VIGAP SA de CV	2016-01-19
OEA PRODUCTORA CLINIMEX INDUSTRIAL S.A. DE C.V.	Productora Clinimex Industrial SA de CV	2016-01-19
FME PRODUCTORA CLINIMEX INDUSTRIAL S.A. DE C.V.	VIGAP SA DE CV	2014-02-21
FME PRODUCTORA CLINIMEX INDUSTRIAL S.A. DE C.V.	Productora Clinimex Industrial SA de CV	2014-02-21