FDA Warning Letter — Howard Phillips LLC dba Phillips Co.

Case 512017 — FEI 3006899835

The FDA took a Warning Letter action against Howard Phillips LLC dba Phillips Co. on May 8, 2017 (Millerton, OK). The action was issued by CDER and concerns drugs products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Howard Phillips LLC dba Phillips Co.
Date
May 8, 2017
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
Millerton, OK (United States)