FDA Warning Letter — Stille AB

Case 418197 — FEI 3003696170

The FDA took a Warning Letter action against Stille AB on Jan 31, 2014 (Torshalla, Sweden). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action details

Facility
Stille AB
Date
Jan 31, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Torshalla (Sweden)

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