FDA Inspection
Healz-Plus, Inc.Healz-Plus, Inc. – FDA Inspection, Nov 29, 2011
Record Details
This FDA Inspection record concerns Healz-Plus, Inc., with an inspection on November 29, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Healz-Plus, Inc.
- Inspection Date
- November 29, 2011
- Product Type
- Drugs
View Company Profile
ID · 6ee060a7-12ac-40d7-b14f-8415cd8ebda6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 755447
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
19- 21 CFR 211.188Prepared for each batch, include complete information
- 21 CFR 211.82(a)Examination on receipt, before acceptance
- 21 CFR 211.82(b)Quarantine Storage of Components
- 21 CFR 211.125(b)Examination of issued labels
- 21 CFR 211.125(f)Procedures Written and Followed
- 21 CFR 211.198(a)Complaint Handling Procedure
- 21 CFR 211.142Written warehousing procedures established/followed
- 21 CFR 211.130Procedures are written, and followed
- 21 CFR 211.186(a)Written procedures followed
- 21 CFR 211.84(d)(2)Reports of Analysis (Components)
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