FDA Warning Letter — Hammill Manufacturing Company

Case 46619 — FEI 3000215103

The FDA took a Warning Letter action against Hammill Manufacturing Company on Jan 6, 2009 (Maumee, OH). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action details

Facility
Hammill Manufacturing Company
Date
Jan 6, 2009
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Maumee, OH (United States)

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