FDA Inspection
Solum & HerbeSolum & Herbe – FDA Inspection, Dec 15, 2011
Record Details
This FDA Inspection record concerns Solum & Herbe, with an inspection on December 15, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Solum & Herbe
- Inspection Date
- December 15, 2011
- Product Type
- Drugs
View Company Profile
ID · 00b48342-0822-42cb-b9b9-275d56ae5ca6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 761039
- FDA center
- Human Drugs
- Project area
- Unapproved and Misbranded Drugs
FDA Citations
9- 21 CFR 211.44Adequate lighting not provided
- 21 CFR 211.188Prepared for each batch, include complete information
- 21 CFR 211.58Buildings not maintained in good state of repair
- 21 CFR 211.63Equipment Design, Size and Location
- 21 CFR 211.198(a)Procedures to be written and followed
- 21 CFR 211.130Procedures are written, and followed
- 21 CFR 211.100(a)Absence of Written Procedures
- 21 CFR 211.56(b)Written sanitation procedures lacking
- 21 CFR 211.22(a)Lack of quality control unit
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