Sturgis Site Fun Facts/History
Project Lighthouse
GMP Trivia
Data Integrity
100

A new Distribution Center was constructed in what year?

What is 1992?
100

Project Lighthouse became effective at the Sturgis, MI site on this day

What is September 1st, 2025?

100

An area that requires the highest level of gowning requirements

What is High Care?

100

Ink must be one of these two colors

What is black or blue?

200

This piece of equipment quadrupled the overall capacity of powder at the plant?

What is Dryer 4?

200

This project type is now obsolete

What is Quality Assessment?

200

GMP guidelines are enforced by this U.S. federal agency

What is the FDA (Food and Drug Administration)?

200

A single one of these must be drawn through incorrect data/information that is being corrected

What is a line?

300

The 1970's saw the creation of this new brand and new category of therapeutic nutritional?

What is Ensure?

300

These are the only two events that get a pNC (Potential Nonconformance) initiated when they occur

What is a leak or NRI?

300

Before entering a GMP area, employees must wash their hands for at least this duration

What is 20 seconds?

300

Controlled postings must be reviewed within this time frame to ensure information is current

What is annually?

400

In the early 1960's, construction of this, significantly increased the powder capacity of the Sturgis plant?

What is Dryer 3?

400

Approval Matrices are located in the back of this procedure

What is AN03-01-002?

400

CAPA stands for Corrective and __ Action

What is Preventive?

400

This acronym outlines the five principles of data integrity

What is ALCOA?

500

Following World War II, Abbott Nutrition was formerly known as this?

What is Moores & Ross Dietetic Company?

500

This allows us to give advance notification of high priority events to our business and allows them to evaluate impact early.

What is a Quality Issue Communication?

500

GMP Work Habits can be found in this Document ID

What is ST-1000.38?

500

This regulation governs the use of electronic records and signatures in GMP environments.

What is 21 CFR Part 11?