FDA Inspection
Plantimex Distributors, Inc.Plantimex Distributors, Inc. – FDA Inspection, Jul 12, 2018
Record Details
This FDA Inspection record concerns Plantimex Distributors, Inc., with an inspection on July 12, 2018, issued by the Center for Food Safety and Applied Nutrition, covering food/cosmetics.
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ID · ce334c65-325a-4159-b7cd-e07077b33c36
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1058687
- FDA center
- Foods & Cosmetics
- Project area
- Colors and Cosmetics Technology
- Outcome
- Form 483 issued
FDA Citations
13- 21 CFR 111.70(d)Specifications - labels, packaging
- 21 CFR 111.453Written procedures - holding
- 21 CFR 111.70(e)Specifications - identity, purity, strength, composition
- 21 CFR 111.16Written procedures - cleaning
- 21 CFR 111.8Written procedures - hygienic practices
- 21 CFR 111.403Written procedures - labeling operations
- 21 CFR 111.553Written procedures - product complaint
- 21 CFR 111.503Written procedures - returned dietary supplement
- 21 CFR 111.165(d)(1)Product received - identify
- 21 CFR 111.465(b)Retain reserve samples - 1 year, 2 years
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Other FDA inspections of Plantimex Distributors, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| June 8, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Plantimex Distributors, Inc.
- FDA Inspection 728887 - 2011-06-08
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