FDA Inspection
RWM Technologies LLCRWM Technologies LLC – FDA Inspection, Oct 4, 2010
Record Details
This FDA Inspection record concerns RWM Technologies LLC, with an inspection on October 4, 2010, issued by the Center for Veterinary Medicine, covering veterinary.
- Company
- RWM Technologies LLC
- Inspection Date
- October 4, 2010
- Product Type
- Veterinary
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ID · e4d2b505-0477-4733-b1b5-430b04844188
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 683732
- FDA center
- Animal Drugs & Feeds
- Project area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
FDA Citations
15- 21 CFR 211.165(d)Acceptance criteria for sampling & testing
- 21 CFR 211.180(b)Record maintenance 1 year (except exempt OTC)
- 21 CFR 211.188(b)(8)Labeling control records including specimens or copies
- 21 CFR 211.188(b)(1)Dates not included for each significant step
- 21 CFR 211.188(b)(13)Examinations for correct labeling
- 21 CFR 211.188(b)(6)Inspection of packaging and labeling area
- 21 CFR 211.188(b)(11)Identification of persons involved, each significant step
- 21 CFR 211.192Quality control unit review of records
- 21 CFR 211.84(d)(2)Reports of Analysis (Components)
- 21 CFR 211.160(a)Lab controls established, including changes
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Other FDA inspections of RWM Technologies LLC
6| Date | Classification | Office | Project area |
|---|---|---|---|
| December 12, 2025 | Not classified | New Orleans District Office | Drug Quality Assurance |
| January 13, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 26, 2019 | NAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| March 6, 2017 | Not classified | New Orleans District Office | |
| September 15, 2015 | NAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
Other documents for RWM Technologies LLC
- FDA Inspection 1294946 - 2025-12-12
- FDA Inspection 1195289 - 2023-01-13
- FDA Inspection 1083930 - 2019-03-26
- FDA Inspection 1004028 - 2017-03-06
- FDA Inspection 942117 - 2015-09-15
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