FDA Inspection
Myson Corporation, Inc.Myson Corporation, Inc. – FDA Inspection, Aug 6, 2013
Record Details
This FDA Inspection record concerns Myson Corporation, Inc., with an inspection on August 6, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Myson Corporation, Inc.
- Inspection Date
- August 6, 2013
- Product Type
- Drugs
View Company Profile
ID · 6ef0761f-ba16-4eba-8483-984e3b59bb0d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 840314
- FDA center
- Human Drugs
- Project area
- Unapproved and Misbranded Drugs
FDA Citations
9- 21 CFR 111.415(f)(1)Batch-lot,control number packaged, labeled dietary supplemen
- 21 CFR 111.83(a)Reserve sample - collect, hold
- 21 CFR 111.80(a)Components packaging, labels used
- 21 CFR 111.70(g)Specifications - finished packaging, labeling
- 21 CFR 111.70(f)Specifications - product received for packaging, labeling
- 21 CFR 111.180(b)(2)Records - receiving; components, packaging, labels, products
- 21 CFR 111.475(b)(1)Written procedures - holding; distributing
- 21 CFR 111.75(c)Specifications met - verify; finished batch
- 21 CFR 111.120(c)Quality control operations - material review, disposition decision
Full citation text and observation details available on the Dashboard.
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.