FDA Inspection
Main Street Casual Living, LLCMain Street Casual Living, LLC – FDA Inspection, Jun 10, 2015
Record Details
This FDA Inspection record concerns Main Street Casual Living, LLC, with an inspection on June 10, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- June 10, 2015
- Product Type
- Devices
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ID · 1ea3691c-a98e-4a02-91b9-6134ac1cfc82
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 929868
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.90(a)Nonconforming product control
- 21 CFR 820.22Quality Audit/Reaudit - conducted
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