Customed, Inc.
CALLE IGUALDAD No. 7, Fajardo, PR, US
Registered product codes
111 product codes
Recent MDR events
2 on file
Recalls
699 on file
- TerminatedApr 14, 2016
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
View FDA record ↗ - TerminatedApr 14, 2016
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
View FDA record ↗ - TerminatedApr 14, 2016
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
View FDA record ↗ - TerminatedApr 14, 2016
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
View FDA record ↗ - TerminatedApr 14, 2016
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
View FDA record ↗ - TerminatedApr 14, 2016
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
View FDA record ↗ - TerminatedApr 14, 2016
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
View FDA record ↗ - TerminatedApr 14, 2016
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
View FDA record ↗ - TerminatedApr 14, 2016
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
View FDA record ↗ - TerminatedApr 14, 2016
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
View FDA record ↗
Compliance history
Matched by FEI 2648727.
FDA inspections
1 on file
- Voluntary Action Indicated (VAI)Oct 4, 2024
Compliance: Devices
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.