FDA Warning Letter — HOYA Corporation PENTAX Miyagi Factory

Case 471414 — FEI 3003782610

The FDA took a Warning Letter action against HOYA Corporation PENTAX Miyagi Factory on Aug 12, 2015 (Kurihara, Japan). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action details

Facility
HOYA Corporation PENTAX Miyagi Factory
Date
Aug 12, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Kurihara (Japan)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.