FDA Warning Letter — Puretone Ltd.

Case 55082 — FEI 3002808722

The FDA took a Warning Letter action against Puretone Ltd. on Apr 10, 2009 (Rochester, United Kingdom). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action details

Facility
Puretone Ltd.
Date
Apr 10, 2009
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Rochester (United Kingdom)

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