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MatOrtho Ltd Form 483 Details

Form 483
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Source: FDA inspection recordConfirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months.

To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3008985661.

MatOrtho Ltd

Leatherhead, -, United Kingdom
Issue DateOctober 22, 2015
FEI Number3008985661
CountryUnited Kingdom
Status
No Warning Letter
Product Type
Devices
MatOrtho Ltd FDA Form 483, Leatherhead, October 22, 2015