# FDA 483 - Deerland Enzymes Inc. - December 23, 2014

Source: https://www.keypedia.com/records/483/deerland-enzymes-inc/ec5a6ec8-0539-47b8-83a4-668e0d011364

> FDA 483 for Deerland Enzymes Inc. on December 23, 2014. Product: other. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Deerland Enzymes Inc.
- Inspection Date: 2014-12-23
- Product Type: other
- Office Name: Atlanta District Office
- Summary: An FDA inspection of Deerland Enzymes Inc., a dietary supplement manufacturer in Kennesaw, GA, revealed significant deficiencies in manufacturing controls and facility sanitation. Observations included the absence of master manufacturing records, inadequate sampling of components, and improper storage of hazardous materials. The inspection also noted repeat observations regarding the accumulation of litter and waste, highlighting persistent issues.

Company: https://www.keypedia.com/companies/deerland-enzymes-inc/c916fdb7-a882-4016-a206-2506d533a305

Office: https://www.keypedia.com/offices/atlanta-district-office/7586d99a-288e-49d1-8c3d-d88b7354b7a7