FDA On-Site Inspection Of Dietary Supplement Manufacturer, Nutramax Laboratories, Inc., Reveals No Deficiencies

Edgewood, MD - The FDA performed a non-scheduled site inspection of Nutramax Laboratories, Inc. in February 2006, which resulted in no deficiencies.

The report notes that this was a comprehensive inspection of manufacturing, packaging, warehouse, sanitation, refrigeration unit, and laboratories, whose functions include product analysis, research and development under the auspices of Nutramax Laboratories, Inc. The inspection was conducted under the cGMPs of 21 CFR 110. The company manufactures high quality, research based, dietary supplements.

The report noted that Nutramax Laboratories, Inc. uses drug GMPs (Good Manufacturing Practices) in the manufacturing of their dietary supplements. An NLEA (Nutrition and Labeling Education Act) exam was performed and again, no deficiencies were found. The findings also note that the company has not had any recalls or regulatory actions against it.

Christine Feaster, director of quality/compliance, states, "We were pleased to welcome FDA to our facility. The inspection was conducted smoothly and efficiently. Its positive outcome is a testament to the quality and commitment of the employees of this company."

SOURCE: Nutramax Laboratories, Inc.