FDA Warning Letter — Techni Med, Inc.

Case 493750 — FEI 3004504906

The FDA took a Warning Letter action against Techni Med, Inc. on Jul 29, 2016 (Aurora, IL). The action was issued by CDER and concerns drugs products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Techni Med, Inc.
Date
Jul 29, 2016
Fiscal Year
2016
Product Type
Drugs
Center
CDER
Location
Aurora, IL (United States)

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